XN330430530 Basic Operation
XN330430530 Basic Operation
XN-L series
XN-530/XN-430
/XN-330
Basic Operation
(North American Edition)
Revision History
12/2016
Software version: Ver. 3
03/2017
Software version: Ver. 3
08/2019
Software version: Ver. 3
04/2020
Software version: Ver. 3
Changes are listed below:
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Revision History
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Table of Contents
Table of Contents
Revision History 3
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Table of Contents
Index 283
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Chapter 1 Basic Operation
Startup ➤P.8
Performing No
instrument handover?
Yes
Have you
No No
Has sample analysis used the instrument
ended for the day? continuously for 24 hours
or more?
Yes Yes
Shutdown ➤P.12
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1.2 Startup
● Instrument inspection
• Check tube and cable connections.
• Check if there are any bent tubes.
• Check if there are any objects on the instrument.
• When connected to a network, make sure that the network devices (hubs and network converters) are all
powered ON.
• Discard any waste fluid in the waste container (if applicable).
● Reagent inspection
Make sure there is a sufficient supply of reagents for the number of samples to be processed that day. Reagent
amounts needed vary by analysis mode. Ready a supply that is slightly greater than the amount you think you
will need that day.
If a reagent runs out during analysis, the instrument will automatically stop. Replace the reagent. Analysis
cannot be resumed until replacement finishes.
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1 Make sure that the main power switches of the instrument and connected
devices are in the ON position.
The main power switch of the analyzer can be kept ON.
Note:
If an error occurs (for example a reagent runs out) during startup, the operator must log on to the
instrument to resolve the error.
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User name
Shutdown button
[IPU Logon] dialog box
Information
In the factory default state, the only user name that appears is [admin] (instrument administrator).
The factory default password for [admin] (instrument administrator) is "m145m".
The administrator should log on as the [admin] and promptly register the users of the instrument and set
their permissions. In addition, change the [admin] password. For details, see Chapter 7.
(➤P.234 "Chapter 7: 7.8.1 User information management (user registration)")
Note:
• If Auto Logon is enabled, the [IPU Logon] dialog box does not appear.
• Display of user names varies depending on the number of users.
• Touch the shutdown button to shut down the instrument.
• Touch [Manual] to display the dialog box to directly enter characters instead of selecting a user name.
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● Background check
Analysis is performed without sample aspiration to check the effectiveness of rinsing. This is repeated up to 3 times.
The analysis results can be checked in the [Data Browser] screen and [Sample Explorer] screen. The
background check data is displayed in [BACKGROUNDCHECK] of the sample number. An analysis value that is
not within the allowable range is marked with [!].
Checked
Background limits Remarks
parameters
WBC 0.10 x 103/μL or less The white blood cell count measured from the WDF channel
6/μL or
RBC 0.02 x 10 less The red blood cell count measured from the RBC/PLT channel
HGB 0.1 g/dL or less -
PLT 10 x 103/μL or less The platelet count measured from the RBC/PLT channel (PLT
distribution)
If the background check results are not within the allowable range after 3 analyses, a background check error
occurs. See "Troubleshooting". (➤Troubleshooting, "Chapter 1: 1.1 Error message list (in alphabetical order)")
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1.3 Shutdown
Shutdown consists of turning OFF the instrument power.
When you finish analysis work for the day, always perform shutdown. If analysis work will continue more than 1 day,
perform shutdown once a day.
2 Make sure that no sample tube remains in the sample tube holder. (XN-530/
XN-430)
On the XN-330, this step is not necessary. Go to step 3.
Information
The sample tube holder retracts immediately before the power turns OFF. The sample tube in the sample
tube holder cannot be removed while the power is OFF.
● XN-530
1 Open the sampler cover (manual
unit).
Note:
If a sample tube remains in the sampler adapter holder, remove it.
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● XN-430
1 If the sample tube holder is not ejected, press the sample tube holder
open/close switch.
Sample tube
[Menu] screen
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Note:
If routine cleaning has not been performed for more than a week,
the dialog box on the right appears. Touch [Yes] to execute routine
cleaning.
For the routine cleaning procedure, see "Troubleshooting".
• XN-530
(➤Troubleshooting, "Chapter 2: 2.4 Executing routine cleaning
(XN-530)" Step 4 and following steps)
• XN-430
(➤Troubleshooting, "Chapter 2: 2.5 Executing routine cleaning (XN-430)" Step 4 and following steps)
• XN-330
(➤Troubleshooting, "Chapter 2: 2.6 Executing routine cleaning (XN-330)" Step 4 and following steps)
5 Touch [OK].
The instrument power automatically turns OFF.
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Information
If a dialog box appears, the screen lock function does not activate after the specified time elapses.
3 Touch [OK].
The screen is released.
Note:
To log off and then log on as a different user, touch [Log on as a different user].
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[Menu] screen
3 Touch [Yes].
The currently logged on user is logged off.
After logoff, the [IPU Logon] dialog box appears. (➤P.9 "1.2.2 Turning ON the power")
Note:
Logoff cannot be executed when the instrument is running.
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Chapter 1 Basic Operation
Toolbar
Contents button
Manual
display area
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Contents display
area
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Button Function
Touch to change the screen to the left or right page.
Touch to move the selected part of a list or the cursor left or right.
Touch to move the selected part of a list or the cursor all the way to the left or to
the right.
Touch to move the selected part of a list or the cursor to the top line or the bottom
line.
Touch an entry field to display a software keyboard or numeric keypad that allows
you to enter characters or numbers.
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Window
(view)
Control menu
Toolbar (fixed) The following frequently-used function buttons are always displayed.
[Menu] Touch to display the [Menu] screen.
(➤P.23 "1.8.2 [Menu] screen")
[QC file] Touch to display the [QC File] screen.
(➤P.105 "Chapter 3: 3.11 [QC File] screen")
[Explorer] Touch to display the [Sample Explorer] screen.
(➤P.175 "Chapter 5: 5.11 [Sample Explorer] screen")
[Browser] Touch to display the [Data Browser] screen.
(➤P.188 "Chapter 6: 6.3 [Data Browser] screen")
Toolbar (variable) The buttons that appear depend on the screen that is displayed.
Window (view) Various tasks are performed and analysis results appear in this area.
In the initial state, the [Menu] screen appears.
Control menu Shows the status of the instrument.
Analysis, maintenance, or other tasks are performed.
(➤P.21 "1.8.1 Control menu")
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Analysis mode
[Manual]/
Indicator Discrete [Sampler]
Control menu
Instrument status Displays the status of the instrument with colors and messages.
The indicated colors have the following meanings.
Green/Orange*: Ready (for analysis) state
Green/Orange blinking*: The instrument is starting up, analyzing, changing
analysis modes, or shutting down.
Green: Waiting to execute maintenance
Green blinking: Executing maintenance
Red: Error (alarm does not sound), initializing system,
emergency stop, inactive
Red blinking: Error (alarm sounds)
* Green in normal conditions, orange when an error that does not require
stopping occurs.
For the sampler analysis mode on the XN-530, the following is shown in
addition to the above.
The starting sample tube position of the next analysis is shown visually.
The rectangle with rounded corners shows the sampler adapter, and the
position is indicated by a white circle.
The starting sample tube position (adapter number and sample tube position) of the
next analysis is shown.
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Printer Displays the printer status. The indicated colors have the following meanings.
status Green: Connected
Red: Printing not possible
Host Displays the status of the host computer connected to the instrument.
computer Becomes orange blinking if a connection error occurs when the instrument is
status set to connect to the host computer.
Becomes gray if the instrument is set to not connect to the host computer.
RU status Shows the status of the RU-20.
Becomes red if an error occurs in the RU-20.
Becomes gray if the instrument is set to not connect to the RU.
Analysis mode Displays the selected analysis mode.
[WB]: Whole Blood mode, [LW]: Low WBC mode, [PD]: Pre-Dilution mode,
[BF]: Body Fluid mode
Discrete Displays the selected discrete.
However, this does not appear when the analysis mode is [BF].
Sample number Displays the sample number.
When [>] appears at the beginning of the sample number, the next sample
can be aspirated. If the sample number was not successfully read, or if the
sample number has not been entered manually, a message is displayed
prompting you to input the number.
Error message Displays the highest priority error among all current errors. The displayed
error is categorized as one of the following error types.
Orange background/black text: Caution
Red background/white text: Warning
Non-urgent information such as notices appear in white text.
[Error] This appears when there is an error.
Touch to display the [Help] dialog box.
[Mode]*1 Touch to select the analysis mode.
The [Change Measurement Mode] dialog box appears.
[Manual]/[Sampler] Varies depending on the analysis method (manual analysis or sampler
analysis*2) and the [Cap Open]*3 setting in the [Manual Analysis] dialog box.
: Displayed when [Cap Open] is OFF in manual analysis mode.
Touch to register sample information and the analysis method for a sample to
be analyzed.
When touched, the [Manual Analysis] dialog box or [Sampler Analysis] dialog
box (when using sampler analysis mode on the XN-530) appears.
*1 This button does not appear in the sampler analysis mode on the XN-530.
*2 XN-530 only.
*3 [Cap Open] is used to specify whether analysis is performed with the sample tube cap open. On the XN-330,
[Cap Open] is always ON.
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Toolbar
Function
category
[Menu] screen
* The icon that appears vary depending on the logged on user permissions.
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3 Touch [OK].
The contents of the [Menu] screen change according to your settings.
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QC QC Analysis
Work List X-barM Setting
Patient List QC File
Rule
Sample Explorer Register Patient Information
Data Browser Register Doctor Name
Instructions for Use Register Ward Name
LOGOFF
Shutdown Calibrator Calibration
Calibration Calibration History
History Precision Check
Setting Precision Check History
Maintenance
Auto Rinse Audit Log
Error Log
Maintenance Log
Reagent Replacement Log Whole Blood Aspiration Motor Test
Sheath Motor Test
Display Settings Aspiration Unit Motor Test
Output Setting Air Pump Test
Data analysis Setting Pinch Valve Test
QC Setting Tube Holder Motor Test
Operational Settings Barcode Reading Test
Instrument Settings Sampler Operation Test
GP Customize
Reagent Replacement
Operation Confirmation
Exchange Drain Waste Fluid Chamber
Rinse Instrument Rinse Waste Fluid Chamber
Status Confirmation Remove Flowcell Air Bubbles
Rinse Flowcell
Drain Reaction Chamber
Drain RBC Isolation Chamber
Remove RBC Detector Clog
Routine Cleaning
Reagent Replenishment
Counter
Sensor
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Chapter 2 Preparation for Analysis (Registering Information)
This chapter explains how to register analysis orders and patient information in the instrument.
If you will be connecting to the host computer and registering information in the host computer, the
procedures in this chapter are not necessary.
Information
If analysis is executed with analysis orders registered in both the instrument and the host computer, the
analysis order registered in the instrument will be used.
Register analysis
No
Register or modify
orders?
Yes
No Register or modify
patient, doctor, or ward
information?
Yes
Analysis registration completed Next step Performing quality control (QC) ➤P.73
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Note:
If 2,000 analysis orders have been registered, the [Regist.] button on the toolbar is grayed out and cannot
be touched. Delete any unneeded analysis orders and then register the new analysis order.
For details on deleting analysis orders, see the following.
(➤P.32 "2.2.3 Deleting analysis orders")
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[FREE SELECT] Use this to select whether each analysis parameter is analyzed.
Touch to display the dialog box on
the right. The parameters that are
displayed depend on your system
configuration.
Select the parameters to be
analyzed.
If the selected parameter
combination does not match the
discretes, [FREE SELECT] is
displayed in the [Discrete] field.
Note:
• If a discrete is not selected under [Discrete], or if the [Sample No.] field is blank or set to "0", [OK] and
[Continuous Registration] are grayed out and cannot be touched.
• If the same information has already been registered in the items below for a different analysis order, an
overwrite confirmation dialog box will appear.
• [Sample No.]
• [Adapter No.]/[Tube Pos.]
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1 Select the analysis order you want to modify in the [Work List] screen.
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4 Touch [OK].
The dialog box closes, and the analysis order is modified.
1 Select the order you want to delete in the [Work List] screen.
Multiple
selection
[Work List] screen (regular display) mode button
Mark displays
Select all
button
Multiple
selection
Select button mode button
Mark displays Orders that are marked (in orange) will be the target of the operation.
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Select button Touch to add marks to the orders on the line where the cursor is positioned.
If a mark already appears, the mark is cleared.
Select all button Touch to add a mark to all orders.
Cancel select all button Touch to clear the marks from all orders.
Multiple selection mode Touch to change the order list to regular mode.
button
3 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
1 Touch the [FIND] button on the toolbar in the [Work List] screen.
The [FIND] dialog box appears.
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[Sample No.] Up to 22 characters can be entered for the condition. Double-byte characters cannot
be entered.
[Patient ID] Up to 16 characters can be entered for the condition. Double-byte characters cannot
be entered.
[Last Name] (the Up to 20 characters can be entered for the condition.
patient's last name)
[First Name] (the Up to 20 characters can be entered for the condition.
patient's first name)
[Ward Name] Up to 20 characters can be entered for the condition.
[Doctor Name] Up to 20 characters can be entered for the condition.
Note:
You can enter "?" and "∗" as wildcard characters in your search.
"?": Used as a wildcard for 1 character.
Example: If you search for "99?99", "99099", "99999", and "99A99" are all selected.
"∗": Used as a wildcard for 0 or more characters.
Example: If you search for "9∗9", "909", "9119", and "99A99" are all selected.
[PREV.] Touch to search upward from the analysis order selected in the list.
[NEXT] Touch to search downward from the analysis order selected in the list.
Note:
Touch [Condition] to return to the dialog box that shows the condition.
4 Touch [Close].
The dialog box closes.
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1 In the [Work List] screen, select the display settings for the analysis order list
you want to print.
For details on changing the list display, see the following.
(➤P.61 "2.4.1 Changing the display method of the analysis order list (display settings)")
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USB memory
stick
USB port
2 Touch the [File] button - [Backup] on the toolbar in the [Work List] screen.
The dialog box on the right appears.
3 Touch [OK].
The backup starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the backup is complete.
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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Note:
If restoring a saved analysis order causes the number of registered analysis orders to exceed 2,000, the
oldest order is automatically deleted.
1 Insert the USB memory stick that contains the pending analysis order
backup file.
Insert the USB memory stick into a free USB port on
the back of the instrument.
A USB memory stick with a password lock function
cannot be used.
USB memory
stick
USB port
2 Touch the [File] button - [Restore] on the toolbar in the [Work List] screen.
The [Import] dialog box appears.
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4 Touch [OK].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the pending analysis order restore is complete.
● When there are analysis orders with the same ordering key
When there is a registered analysis order with
the same ordering key content as the ordering
key of an analysis order being restored, the
dialog box on the right appears.
• To delete the registered analysis order and
restore the analysis order in the backup file
Touch [Yes].
• To not restore the analysis order with the Example: When the ordering key is a sample
matching ordering key number
Touch [No].
• To cancel the restore
Touch [Cancel].
Select the [Apply All] checkbox to take the same action for all further analysis orders with the same
ordering keys.
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Note:
If a new patient is registered when 10,000 patients have already been registered, the patient information
with the oldest update date and time is automatically deleted.
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Note:
If patient information with the same [Patient ID] has already been registered, an overwrite confirmation
dialog box will appear.
1 Select the patient you want to modify or delete in the [Register Patient
Information] screen.
Details
button
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Note:
When the details button is touched, the detailed information of the selected patient appears below the list.
3 Touch [OK].
The dialog box closes, and the patient information is modified.
● To delete
2 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
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1 Touch the [FIND] button on the toolbar in the [Register Patient Information] screen.
The [FIND] dialog box appears.
[Patient ID] Up to 16 characters can be entered for the condition. Double-byte characters cannot
be entered.
[Last Name] (the Up to 20 characters can be entered for the condition.
patient's last name)
[First Name] (the Up to 20 characters can be entered for the condition.
patient's first name)
Note:
You can enter "?" and "∗" as wildcard characters in your search.
"?": Used as a wildcard for 1 character.
Example: If you search for "99?99", "99099", "99999", and "99A99" are all selected.
"∗": Used as a wildcard for 0 or more characters.
Example: If you search for "9∗9", "909", "9119", and "99A99" are all selected.
[PREV.] Touch to search upward from the patient information selected in the list.
[NEXT] Touch to search downward from the patient information selected in the list.
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Note:
Touch [Condition] to return to the dialog box that shows the condition.
4 Touch [Close].
The dialog box closes.
Note:
To save patient information, ward names, or doctor names in CSV format, the [Output patient information]
checkbox must be selected in the [Security] settings. For details on the security, see Chapter 7.
(➤P.251 "Chapter 7: 7.9.3 Security settings")
Follow the steps below to save the patient information in CSV format.
USB memory
stick
USB port
2 Touch the [File] button - [Output in CSV Format] on the toolbar in the
[Register Patient Information] screen.
The data save starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the data save is complete.
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* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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[No.] The minimum number that has not been registered is automatically generated. This
number can be changed.
A number between 1 and 200 can be entered.
[Ward Name] Enter a ward name.
Up to 20 characters can be entered.
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Note:
If a ward name with the same [No.] has already been registered, an overwrite confirmation dialog box will
appear.
1 Select the ward you want to modify or delete in the [Register Ward Name]
screen.
3 Touch [OK].
The dialog box closes and the ward name is modified.
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● To delete
2 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
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1 Touch the [FIND] button on the toolbar in the [Register Ward Name] screen.
The [FIND] dialog box appears.
Note:
You can enter "?" and "∗" as wildcard characters in your search.
"?": Used as a wildcard for 1 character.
Example: If you search for "99?99", "99099", "99999", and "99A99" are all selected.
"∗": Used as a wildcard for 0 or more characters.
Example: If you search for "9∗9", "909", "9119", and "99A99" are all selected.
[PREV.] Touch to search upward from the ward name selected in the list.
[NEXT] Touch to search downward from the ward name selected in the list.
Note:
Touch [Condition] to return to the dialog box that shows the condition.
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4 Touch [Close].
The dialog box closes.
Note:
To save patient information, ward names, or doctor names in CSV format, the [Output patient information]
checkbox must be selected in the [Security] settings. For details on the security, see Chapter 7.
(➤P.251 "Chapter 7: 7.9.3 Security settings")
The procedure is the same as for saving patient information in CSV format. See the following.
(➤P.44 "2.3.4 Saving patient information in CSV format")
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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[No.] The minimum number that has not been registered is automatically generated.
This number can be changed. A number between 1 and 200 can be entered.
[Doctor Name] Enter a doctor name.
Up to 20 characters can be entered.
Note:
If a doctor name with the same [No.] has already been registered, an overwrite confirmation dialog box will
appear.
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1 Select the doctor you want to modify or delete in the [Register Doctor Name]
screen.
3 Touch [OK].
The dialog box closes and the doctor name is modified.
● To delete
2 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
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Note:
To save patient information, ward names, or doctor names in CSV format, the [Output patient information]
checkbox must be selected in the [Security] settings. For details on the security, see Chapter 7.
(➤P.251 "Chapter 7: 7.9.3 Security settings")
The procedure is the same as for saving patient information in CSV format. See the following.
(➤P.44 "2.3.4 Saving patient information in CSV format")
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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USB memory
stick
USB port
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5 Touch [OK].
The backup starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the backup is complete.
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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Note:
If restoring saved information causes the number of registered items of any of the types of information to
exceed the maximum, the oldest item is automatically deleted.
1 Insert the USB memory stick that contains the patient, ward, or doctor
information backup file.
Insert the USB memory stick into a free USB port on
the back of the instrument.
A USB memory stick with a password lock function
cannot be used.
USB memory
stick
USB port
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2 Touch [OK].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the information restore is complete.
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Select the [Apply All] checkbox to take the same action for all further cases where a control number is the
same but the information is different.
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Toolbar
Analysis order
list
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2.4.1 Changing the display method of the analysis order list (display
settings)
You can change the sorting order of the analysis order list, and specify filter conditions to display only specific
analysis orders.
Follow the steps below to change the display method.
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[No Display Settings] Touch to change to the standard display method (sort conditions: date and time of
registration in ascending order, filter conditions: none).
[Pending] Touch to display only pending analysis orders.
[Display Settings 1], Touch to change to the sort conditions and filter conditions set in the corresponding
[Display Settings 2] item.
[Setting] Touch to set the sort conditions and filter conditions.
The name of the selected display method appears next to the screen name in the upper left corner of the screen.
[Date] Sorts by the date and time the data was registered.
[Sample No.] Sorts by sample number.
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[Status] [PEND.] —
[COMP.]
[ERR.]
6 Touch [Regist.].
The dialog box closes and the set information is registered. The list display changes according to the set
conditions.
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Toolbar
Details button
Patient information
list
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[Patient Name] Displays the name of the patient (first name and last name).
[Sex] Displays the patient's sex.
Details button Touch to display the detailed information of the patient selected in the patient
information list below the list.
Detailed information
1 Touch the [Display] button on the toolbar in the [Register Patient Information]
screen.
The submenu on the right appears.
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[No Display Settings] Touch to change to the standard display method (sort conditions: patient ID in
ascending order, filter conditions: none).
[Display Settings 1] Touch to change to the sort conditions and filter conditions that have been set.
[Setting] Touch to set the sort conditions and filter conditions.
The name of the selected display method appears next to the screen name in the upper left corner of the screen.
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6 Touch [Regist.].
The dialog box closes and the set information is registered. The list display changes according to the set
conditions.
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2.6.1 Changing the sorting order of the ward name list (display
settings)
The sorting order of the ward name list can be changed.
Follow the steps below to sort a ward name.
1 Touch the [Display] button on the toolbar in the [Register Ward Name] screen.
The submenu on the right appears.
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2.7.1 Changing the sorting order of the doctor name list (display settings)
The sorting order of the doctor name list can be changed.
The procedure is the same as for changing the sorting order of the ward name list. See the following.
(➤P.69 "2.6.1 Changing the sorting order of the ward name list (display settings)")
The sort keys are the number and the doctor name.
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Chapter 3 Performing Quality Control (QC)
3.1 Flow of QC
The flow chart below shows the sequence of QC. The typical flow is shown in gray.
Perform QC
XN-530 XN-430/XN-330
No Yes
Has the control lot Has the control lot
been registered? been registered?
No
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3.2 Overview of QC
QC is the routine monitoring of instrument and reagent performance using control blood or normal samples.
Variations of the analysis results are compared daily. When the changes in performance to be detected are
significant, you must take action, such as calibration.
3.2.1 Types of QC
The QC techniques below can be used. Use the appropriate method according to your needs.
● Samples used in QC
QC materials and QC methods are shown below.
* Only when the instrument has the body fluid analysis function.
Information
When performing X-bar control or L-J control, use the specified control blood only. Control blood is
specifically tailored to the analysis technology of the instrument.
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Note:
You can have a message displayed at a selected interval to prompt the operator to perform QC (QC alarm).
For details on the QC alarm settings, see Chapter 7.
(➤P.229 "Chapter 7: 7.7.2 QC alarm settings")
3.2.3 QC files
A QC file is a file in which QC analysis results are saved by control blood lot.
The instrument has 99 QC files. L-J control or X-bar control data can be saved in QC file numbers QC01 to
QC96. QC file numbers QC97 to QC99 are used for X-barM control, and QC data of CBC, DIFF, and RET* are
saved in that order.
Before performing QC analysis for the first time, or before performing QC analysis with a new control blood, a
QC file must be selected and lot information must be registered.
For details on registering lot information, see the following.
• To register lots automatically in sampler analysis (XN-530 only)
(➤P.77 "3.4 Registering lots automatically (XN-530)")
• Other cases
(➤P.78 "3.5 Registering lots")
* QC file QC99 cannot be used when the instrument does not have the RET analysis function.
Note:
• When registering lots automatically on the XN-530, the QC file with the lowest number that does not
have lot information registered is selected. If all QC files have lot information registered, the data in the
unused file with the oldest lot registration date is deleted, and the lot information is registered in that file.
• A maximum of 300 QC analysis results are saved in a QC file. When 300 analysis results are exceeded,
the analysis result with the oldest date and time is automatically deleted.
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Information
• In the cases below, QC analysis cannot be performed in sampler analysis mode. Perform QC analysis in
manual analysis mode.
• X-bar control
• QC of body fluid analysis
• To perform QC analysis in sampler analysis mode, barcodes must be used. For the barcode reader
settings, see Chapter 7.
(➤P.252 "Chapter 7: 7.9.4 Barcode reader settings (XN-530)")
Note:
Lot information (expiration date, target value, limit value) is acquired from the assay file using the lot
number as key. The acquired information is registered in the file with the lowest file number that does not
have a file registered in QC files* QC01 to QC96.
* Excluding files selected in the [QC File] screen or the [QC Chart] screen.
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USB memory
stick
USB port
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4 Touch [OK].
The contents of the selected assay file are read and set in the items.
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Manual settings
The value of the analysis parameter selected in the target value/limit value list appear in [Target] or [Limit Range
(#)] on the right side of the dialog box. Enter values in the input fields on the right side to set the target value and
limit value for each analysis parameter.
● [Variable Target]
This function automatically calculates and sets the target value from the QC analysis results.
The target value is the average value of the analysis results, excluding the most recent result.
When the number of analysis results is zero: 0
If [Limit Setting] is [Ratio (%)], the limit range will be
100% and the minimum number of significant digits
for each QC parameter will appear on the grid.
For details on [Limit Setting], see Chapter 7.
(➤P.228 "Chapter 7: 7.7.1 QC settings")
When the number of analysis results is 1: That value
When the number of analysis results is 2 or more: The average value, excluding the most recent
analysis result
If a "0" is entered in [Target] or it is left blank, it will be processed as a variable target.
If you want to change the target value of the selected analysis parameter to a variable target, touch
[Variable Target]. The target value of the selected analysis parameter changes to the un-entered state. To
change the target values of all analysis parameters to a variable target, select the [Select All] checkbox and
touch [Variable Target].
[Auto Settings]
The target value and limit range can be set using any QC analysis result.
This function cannot be used when registering a lot.
For details on the auto settings, see the following.
(➤P.99 "3.10.1 Modifying lot information")
7 Touch [OK].
The [Target/Limit Settings] dialog box closes and you return to the [Input Lot Information] dialog box.
Information
If [Material] is changed, the contents of the [Target/Limit Settings] dialog box are reset to the values that
appeared when the [Input Lot Information] dialog box was displayed.
8 Touch [OK].
The set information is registered and the [Input Lot Information] dialog box closes.
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Information
• In the cases below, QC analysis cannot be performed in sampler analysis mode. Perform QC analysis in
manual analysis mode. (➤P.83 "3.6.2 Performing QC analysis in manual analysis mode (XN-530)")
• X-bar control
• QC of body fluid analysis
• If you are not using barcodes.
• To perform QC analysis in sampler analysis mode, barcodes must be used. For the barcode reader
settings, see Chapter 7.
(➤P.252 "Chapter 7: 7.9.4 Barcode reader settings (XN-530)")
Before performing QC analysis for the first time, or before performing QC analysis with a new control blood, a
QC file must be selected and lot information must be registered.
For details on registering lot information, see the following.
• Automatic registration when performing sampler analysis (XN-530 only)
(➤P.77 "3.4 Registering lots automatically (XN-530)")
• Other cases
(➤P.78 "3.5 Registering lots")
Place the vial containing the control blood in the sampler adapter, and analyze the control blood in sampler
analysis mode.
For the analysis procedure, see Chapter 4.
(➤P.124 "Chapter 4: 4.4 Analyzing samples using sampler analysis (XN-530)")
Check the QC analysis results in the radar chart of the [QC File] screen or in the [QC Chart] screen. For the
checking procedure, see the following.
(➤P.93 "3.7 Checking analysis results")
Note:
• If QC is performed with multiple differing lots, the vials of the lots can be placed together in the sampler
adapter to perform multiple QC analyses in 1 sampler analysis run.
• If you want to perform normal analysis immediately after QC analysis, place the sample for normal
analysis in the sampler adapter with the vials and start analysis. Place the sample tube for normal
analysis in the position that will be analyzed after the vials.
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Caution!
The instrument does not mix the control blood. Be sure to perform mixing immediately before starting
analysis.
Before performing QC analysis for the first time, or before performing QC analysis with a new control blood, a
QC file must be selected and lot information must be registered.
For details on registering lot information, see the following.
(➤P.78 "3.5 Registering lots")
2 Make sure the button on the right edge of the control menu is [Manual]. When
the mode is set to [Sampler], press the mode switch.
The mode changes to manual analysis mode.
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5 Touch [OK].
The dialog box closes.
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QC file
list
8 From the QC file list, touch the file you want to analyze.
The dialog box* below appears.
* The analysis parameters that appear vary depending on your system configuration and the type of QC file.
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Note:
If a low control blood or other error occurs during analysis, an alarm will sound. To stop the alarm, touch
any place on the touchscreen. A [Help] dialog box with information on the error cannot be opened until
analysis finishes. For details on [Help] dialog box, see "Troubleshooting". (➤Troubleshooting, "Chapter 1:
1.2 [Help] dialog box")
11 Touch [Accept].
The analysis results are saved in the QC file and the dialog box closes.
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Note:
• To close the dialog box without saving the analysis results in the QC file, touch [Cancel].
• Regardless of whether or not the analysis results are saved in the QC file, they are saved as analysis
result data in the [Sample Explorer] screen when analysis finishes.
Check the detailed analysis results in the radar chart of the [QC File] screen or in the [QC Chart] screen.
For details on checking the analysis results, see the following.
(➤P.93 "3.7 Checking analysis results")
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Caution!
The instrument does not mix the control blood. Be sure to perform mixing immediately before starting
analysis. Follow the instructions included in the package insert of the quality control material for information
on the mixing procedure.
Before performing QC analysis for the first time, or before performing QC analysis with a new control blood, a
QC file must be selected and lot information must be registered.
For details on registering lot information, see the following.
(➤P.78 "3.5 Registering lots")
2 If the sample tube holder is not ejected, press the sample tube holder
open/close switch. (XN-430)
The sample tube holder is ejected.
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5 Touch [OK].
The dialog box closes.
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QC file
list
8 From the QC file list, touch the file you want to analyze.
The dialog box* below appears.
* The analysis parameters that appear vary depending on your system configuration and the type of QC file.
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Note:
If a low control blood or other error occurs during analysis, an alarm will sound. To stop the alarm, touch
any place on the touchscreen. A [Help] dialog box with information on the error cannot be opened until
analysis finishes. For details on [Help] dialog box, see "Troubleshooting". (➤Troubleshooting, "Chapter 1:
1.2 [Help] dialog box")
11 Touch [Accept].
The analysis results are saved in the QC file and the dialog box closes.
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Note:
• To close the dialog box without saving the analysis results in the QC file, touch [Cancel].
• Regardless of whether or not the analysis results are saved in the QC file, they are saved as analysis
result data in the [Sample Explorer] screen when analysis finishes.
Check the detailed analysis results in the radar chart of the [QC File] screen or in the [QC Chart] screen.
For details on checking the analysis results, see the following.
(➤P.93 "3.7 Checking analysis results")
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1 In the [QC Chart] screen, move the cursor to the data that was analyzed with
the new vial.
Touch the chart to move the cursor to data near that position.
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1 Touch the [Range] button on the toolbar in the [QC Chart] screen.
Range selection mode is activated, and a sub-cursor appears on the QC chart.
The sub-cursor is fixed at the position where the main cursor was located to indicate the start point of the range
selection.
2 Touch the end point of the range you want to Main cursor Sub-cursor
select on the QC chart.
The main cursor is moved to that point, and the range between
the sub-cursor and the main cursor is selected.
Selected range
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Note:
To delete all QC file data (including lot registration information), see the following.
(➤P.101 "3.10.3 Deleting QC file data")
1 Select the analysis result you want to delete in the [QC Chart] screen.
To delete 1 analysis result, move the cursor to the analysis result you want to delete. Touch the chart to move
the cursor to data near that position.
To delete a selected range of multiple analysis results, change to range selection mode and select the range.
For the range selection procedure, see the following.
(➤P.95 "3.7.3 Selecting the QC analysis result range")
3 Touch [Yes].
The selected analysis results are deleted.
The relationship between the vial line and plotted points is as follows.
(1) (2)
Delete
Delete
Delete
The plotted
(2) points before
and after the
Old vial line deleted points
Vial line is not
is not are connected
displayed
displayed by the line
All plotted points in front of the All plotted points between the Plotted points before and after
vial line are deleted vial lines are deleted the vial line are deleted
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Note:
The instrument can be set to automatically output QC analysis results to the host computer or a printer. For
details, see Chapter 7. (➤P.243 "Chapter 7: 7.8.6 Auto output settings")
1 Select the analysis results you want to output in the [QC Chart] screen.
To output 1 analysis result, move the cursor to the analysis result you want to output. Touch the chart to move
the cursor to data near that position.
To output a selected range of multiple analysis results, change to range selection mode and select the range.
For the range selection procedure, see the following.
(➤P.95 "3.7.3 Selecting the QC analysis result range")
2 Touch the output destination from the [Output] button on the toolbar.
Destinations that are not connected are grayed out and cannot be selected.
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4 Touch [OK].
X-barM control ON or OFF is set.
Note:
You can check whether X-barM control is ON or OFF in the Xm status in the control menu.
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Note:
[Material] cannot be changed, and thus the [Read Assay File] is grayed out and cannot be selected.
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3 Touch [OK].
The modified settings are saved.
1 In the [QC Chart] screen, move the cursor to the desired analysis result.
Touch the QC chart to move the cursor to data near that position.
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4 Touch [OK].
The set information is applied to the cursor data.
1 In the [QC File] screen, select the QC file that contains the data you want to
delete.
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3 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
The data of the QC file is deleted, and the file changes to the lot un-registered state.
Note:
X-barM control data cannot be backed up.
USB memory
stick
USB port
2 In the [QC File] screen, select the QC file that contains the data you want to
save.
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* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
1 Insert the USB memory stick that contains the backup file.
Insert the USB memory stick into a free USB port on
the back of the instrument.
A USB memory stick with a password lock function
cannot be used.
USB memory
stick
USB port
Note:
A file cannot be restored if a QC file with the same lot number already exists.
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2 Touch [OK].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the QC file data restore is complete.
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Toolbar
QC file
list
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Radar charts
QC file
list
QC analysis results
The radar charts that appear vary
depending on your system configuration
and the type of QC file.
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3.11.1 Changing the display method of the QC file list (display settings)
You can change the sorting order of the QC file list, and specify filter conditions to display only specific QC files.
Follow the steps below to change the display method.
[All Files] Touch to change to the standard display method (sort conditions: file number in
descending order, filter conditions: none).
[Display Settings 1] to Touch to change to the sort conditions and filter conditions that have been set.
[Display Settings 3]
[Setting] Touch to set the sort conditions and filter conditions.
The name of the selected display method appears next to the screen name in the upper left corner of the screen.
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6 Touch [Regist.].
The dialog box closes and the set information is registered. The list display changes according to the set
conditions.
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Toolbar
QC file
information
QC chart
display
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[Output] Touch to open a submenu that allows you to output the QC analysis results
selected in the QC chart display to the output destination shown in the submenu.
(➤P.97 "3.8 Outputting QC analysis results to the host computer or a printer")
[Range] Touch to change the QC chart to range selection mode.
(➤P.95 "3.7.3 Selecting the QC analysis result range")
[File] Touch to open a submenu that allows you to save or restore all data in the QC
file.
[Backup]: Use to back up the QC file data.
(➤P.102 "3.10.4 Saving QC file data (backup)")
[Restore]: Use to restore the backed up data.
(➤P.103 "3.10.5 Restoring saved data
(restore)")
[Output in SNCS Format]: Use to save the data in SNCS format.
[Output in Sysmex Insight]: Use to save the data in Sysmex Insight format.
Select a QC file that does not have a lot registered in the [QC File] screen and
restore data.
X-barM control data cannot be backed up or restored.
[Delete] Use to delete the QC analysis results selected in the QC chart.
(➤P.96 "3.7.4 Deleting analysis results")
QC file information Displays lot information (file number, expiration date, material, QC analysis
sample number).
If the control blood has expired, the expiration date appears in white on a red
background.
The QC analysis sample number is the lot number with [QC-] added.
An X-barM control QC file is shown as follows.
File number: [X-barM]
Expiration date: Blank
Material: Discrete ([CBC]/[DIFF]/[RET])
QC sample number: Blank
QC chart display Displays the QC analysis results.
[Item] Displays the analysis parameter name.
[UL] Displays the limit value (upper).
[Target] Displays the target value.
[LL] Displays the limit value (lower).
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QC chart The QC analysis results are plotted over time and displayed as a broken-line
graph.
Comment display
area
Comment marks
Plot points
Vial line
Calibration line
Main cursor
Analysis date
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This is a line for selection of QC analysis results. Touch the QC chart to move
the line to a QC analysis result near the touched point.
The analysis result that is selected by this line is called cursor data.
Main cursor When range selection mode is activated, the main cursor changes to the
sub-cursor (fixed line) and a new main cursor appears. The range of QC
analysis results between the main cursor and sub-cursor can be selected.
For the range selection procedure, see the following.
(➤P.95 "3.7.3 Selecting the QC analysis result range")
[Data] Displays the cursor data value.
In range selection mode, the data value indicated by the sub-cursor is shown.
If outside the limit range, the value is shown in white on a red background. If
above the upper limit, [+] appears to the left of the value. If under the lower limit,
[-] appears to the left of the value.
[SD] Displays the standard deviation calculated from all managed QC analysis
results.
If there is only one result, this cannot be calculated and [- - - -] appears.
When range selection mode is activated, this is calculated from the managed
data inside the range.
[Mean] Displays the mean value calculated from all managed QC analysis results.
When range selection mode is activated, this is calculated from the managed
data inside the range.
[CV] Displays the coefficient of variation calculated from all managed QC analysis
results.
If there is only one result, this cannot be calculated and [- - - -] appears.
When range selection mode is activated, this is calculated from the managed
data inside the range.
[n=] Displays the number of QC analysis results that are managed.
When range selection mode is activated, the number of managed analysis
results inside the range is shown.
Note:
• If the displayed range of the QC chart contains plotted points that are excluded from control, the plotted
points are not connected to the plotted points outside the displayed range.
Current display range Current display range
Lines are not connected. Lines are not connected. Lines are not connected.
• Plotted points that show [- - - -] or a data mask indicating non-analyzable are not joined by lines. For
details on data masks, see Chapter 5.
(➤P.180 "Chapter 5: 5.11.2 Display of analysis result data")
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3 Touch [Move Up] or [Move Down] to move the analysis parameter to the
desired position.
To move a different analysis parameter, touch the analysis parameter and then touch [Move Up] or [Move Down]
in the same way.
4 Touch [OK].
The QC chart display changes to the set order.
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4 Touch [OK].
The data of only the selected shift is displayed.
[Shift All] in the submenu changes to the name of the selected shift.
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Analyze samples
Yes
Analyze samples ➤P.143
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Caution!
• Before placing the sample in the sample holder or sampler tube adapter (XN-530 only), check to make
sure that the sample is sufficiently mixed. Exercise particular caution if the sample settles quickly or has
been stored in a cooler or low-temperature environment.
• Do not analyze coagulated blood.
• The instrument is equipped with an aspiration sensor. However, there is a possibility that correct results
may not be obtained if the sample volume is low and the sensor is not able to detect blood aspiration
error.
• While analysis is in progress, do not remove/insert the hand-held barcode reader or turn OFF the main
power switch on the instrument. Risk of corruption of the information that is written to the reagent cartridge.
If you accidentally remove or insert the hand-held barcode reader during analysis, restart the instrument to
reset.
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4.2.3 Discrete
Discretes are groups of analysis parameters.
Analysis parameters can be specified in an analysis order by selecting a discrete group rather than individual
analysis parameters.
Discrete selected in
Remarks
analysis order
CBC —
CBC+DIFF —
CBC+RET Cannot be selected when the instrument does not have the RET analysis function.
CBC+DIFF+RET Cannot be selected when the instrument does not have the RET analysis function.
FREE SELECT Appears when individual analysis parameters are specified in the [Work List].
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* The availability of [Low WBC] mode and [Body Fluid] mode depends on your system configuration.
Caution!
• Before placing the sample in the sample holder or sampler tube adapter (XN-530 only), check to make
sure that the sample is sufficiently mixed. If too much time elapses from mixing until analysis, there is a
risk that correct analysis results will not be obtained.
Exercise particular caution if the sample settles quickly or has been stored in a cooler or low-temperature
environment.
• Use only the specified anticoagulant.
Using a non-specified anticoagulant may result in hemolysis or platelet aggregation, preventing correct
analysis results.
• When analyzing in [Low WBC] mode, mix the sample gently and analyze promptly. Excessive mixing or
the elapse of time may cause incorrect results.
• When using sample tubes, follow the instructions on the sample tube package insert.
If the sample volume is greater than the specified volume, correct analysis results may not be obtained
due to insufficient mixing or sample coagulation.
When the sample volume is normal, there will be a layer of air at the top of the sample tube.
When there is no air layer, the sample will not mix when the sample tube is turned over. Check the
sample volume before mixing.
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* This instrument has a CELLPACK DCL dispensing function. For the dispensing procedure, see the following.
• XN-530:
(➤P.148 "4.8.1 Preparing diluted blood with the diluent dispensing function (XN-530)")
• XN-430:
(➤P.152 "4.8.2 Preparing diluted blood with the diluent dispensing function (XN-430)")
• XN-330:
(➤P.155 "4.8.3 Preparing diluted blood with the diluent dispensing function (XN-330)")
Caution!
• Do not dilute to other than the specified dilution ratio. Otherwise you will obtain incorrect analysis results.
• The sample should be analyzed immediately after dilution, as platelet aggregation can easily occur in
diluted samples.
In addition, the dispensed diluent can cause a certain amount of error in the analysis values due to
evaporation and contamination. For this reason, a new diluted blood sample should be prepared for each
analysis.
• After diluting the sample, mix gently and analyze promptly. If the sample is mixed excessively after dilution, the
results may not be accurate.
• It is acceptable to apply light pressure when collecting a capillary blood sample. However, too much pressure
will force body fluid into the blood and lower the reliability of the analysis results.
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Caution!
• Mix the sample gently after collection.
• Excessive mixing of a body fluid sample may cause false high values at WBC-BF and TC-BF#.
• Fat globules, crystals, high viscous synovial fluids, bacterium, and fungi may cause erroneous or misleading
results.
• Failure to properly collect, store and transport specimens may compromise results. Sysmex recommends that
you follow CLSI guidance documents or equivalent procedures.
• WBC-BF counts < 0.004 x 103/μL or RBC-BF counts < 0.002 x 106/μL should be confirmed using an alternate
method.
• The laboratory should perform additional testing if more specific or sensitive limitation information is needed.
● Sample volume
Aspirated sample volumes and required sample volumes are indicated below.
XN-530/XN-430
Aspirated Required
Analysis method Specimen Sample tube Cap sample sample
volume volume
Sampler analysis Whole blood Regular sample tube Closed tube 25 µL 1 mL
(XN-530) RBT micro collection Closed tube 250 µL
tube
Manual analysis Whole blood Regular sample tube Closed tube 25 µL 1 mL
Open tube 300 µL
RBT micro collection Closed tube 250 µL
tube
Micro collection tube Open tube 100 µL
Diluted Regular sample tube Open tube 70 µL 300 µL
blood Micro collection tube Open tube 140 µL
Body fluid* Regular sample tube Closed tube 70 µL 1 mL
Open tube 300 µL
Micro collection tube Open tube 140 µL
* The availability of the body fluid analysis function depends on your system configuration.
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XN-330
Aspirated
Analysis method Specimen Sample tube Cap sample
volume
Manual analysis Whole blood Regular sample tube Open tube 25 µL
Diluted blood Regular sample tube Open tube 70 µL
*
Body fluid Regular sample tube Open tube 70 µL
* The availability of the body fluid analysis function depends on your system configuration.
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Caution!
• If the sample is left sitting for more than 4 hours and the blood cells and plasma separate, correct analysis
results may not be obtained due to insufficient mixing.
To analyze this type of sample, mix the blood sufficiently before placing the sample in the sampler adapter.
• When using sample tubes, follow the instructions on the sample tube package insert.
If the sample volume is greater than the specified volume, correct analysis results may not be obtained due to
insufficient mixing or sample coagulation.
• When the sample volume is normal, there will be a layer of air at the top of the sample tube.
When there is no air layer, the sample will not mix when the sample tube is turned over. Check the sample
volume before mixing.
1 Make sure that the sampler cover (front) and the sampler cover (manual unit)
are closed.
If either is open, close it. Sampler cover (front)
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2 Make sure the button on the right edge of the control menu is [Sampler].
When the mode is set to [Manual], press the mode switch.
The mode changes to sampler analysis mode.
Note:
In sampler analysis mode, instrument status of the
control menu switches to the state as shown on the right. (1)
(1) The starting sample tube position of the next
analysis is shown visually. The rectangle with (2)
rounded corners shows the sampler adapter, and
the position is indicated by a white circle.
(2) The starting sample tube position (adapter number
and sample tube position) of the next analysis is
shown. Control menu
And the button on the right edge of the control menu
changes to [Sampler].
3 Make sure that either the left or right sampler adapter holder is in a state
where it can be pulled out.
A sampler adapter holder can be pulled out when the sampler
adapter status indicator LED is as follows.
• Solid green
• OFF
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4 Pull out the sampler adapter holder that you want to use.
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Caution!
Use the appropriate sampler adapter for the sample tube.
If an unsuitable adapter is used, aspiration problems may cause incorrect analysis results, and instrument
damage may occur.
For the types of sampler adapters, see "General Information".
(➤General Information, "Chapter 5: 5.3.3 Supported sampler adapter")
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[Starting Tube Position] Pull out the sampler adapter holder that you want to use.
[Sample No.] Set the number of the sample in the starting sample tube position. The [Sample
No.] of each sample tube from the second tube on is determined by automatically
incrementing the previous number.
When querying for the analysis order using barcodes, this does not need to be set.
[Discrete] Set the analysis discrete for the sample in each sample tube position.
When querying for the analysis order using barcodes, this does not need to be
set.
[Adapter No.] Set the adapter number of the sampler adapter with the sample tube from which
analysis will start.
The [Adapter No.] of the sampler adapter that will be analyzed afterward will be
assigned by automatically incrementing the adapter number.
Note:
Analysis takes place in the order of the sampler adapter sample tube positions, starting from the analysis
start position set in [Starting Tube Position] in the [Sampler Analysis] dialog box.
If 2 sampler adapters are set and analysis is started with [Starting Tube Position] set to the 1st position of
the left adapter, the order of analysis will be as shown below.
10 9 8 7 6 20 19 18 17 16
5 4 3 2 1 15 14 13 12 11
Sampler adapter set in the sampler Sampler adapter set in the sampler
adapter holder (left) adapter holder (right)
10 Touch [OK].
The dialog box closes, and the analysis order is set.
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11 Place the sampler adapter in the sampler adapter holder selected in the
[Sampler Analysis] dialog box.
You can also check whether the left or right sampler Sampler adapter
adapter is selected in the instrument status in the
control menu.
Attach the sampler adapter in the orientation shown
in the illustration.
Top view
Note:
If the instrument is set to perform retesting, it will automatically analyze the sample multiple times.
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14 Pull out the analyzed sampler adapter holder, and remove the sampler adapter.
If you are using 2 sampler adapters for sampler analysis, 1 sampler adapter holder can be opened and closed
even while analysis of the other sampler adapter is in progress.
16 If you have another sample to analyze, place the sampler adapter in the
sampler adapter holder.
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Caution!
• The instrument does not mix the sample. Be sure to perform mixing immediately before starting analysis.
• Analysis cannot be performed in [Pre-Dilution] mode or [Body Fluid] mode when an RBT micro collection
tube is used.
1 Make sure the button on the right edge of the control menu is [Manual]. When
the mode is set to [Sampler], press the mode switch.
The mode changes to manual analysis mode.
Note:
If the mode switch is pressed while analysis is in progress in sampler analysis mode, sampler analysis will
pause when analysis of the current sample is completed, and the mode will change to manual analysis mode.
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3 If you want to change the analysis mode, touch [Mode] in the control menu.
The [Change Measurement Mode] dialog box appears.
The analysis modes that appear depend on your system
configuration.
5 Touch [OK].
The dialog box closes.
Checked
Background limits Remarks
parameter
WBC-BF 0.001 x 103/μL or White blood cell counts in body fluid measured from the
less WDF channel
RBC-BF 0.003 x 106/μL or Red blood cell counts in body fluid measured from the
less RBC/PLT channel
If the results are not within the allowable range after 3 analyses, a background check error occurs. See
"Troubleshooting". (➤Troubleshooting, "Chapter 1: 1.1 Error message list (in alphabetical order)")
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Note:
If the sample number is set to [Automatically increment Sample No. (manual mode)] and the analysis
settings are the same as the previously analyzed sample, settings of this dialog box can be omitted. For
details on auto increment of sample numbers, see Chapter 7.
(➤P.241 "Chapter 7: 7.8.4 Sample number auto increment settings")
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[Patient Information] Touch [Input] to enter the patient ID with the software keyboard.
If the patient information of the entered patient ID is registered in the instrument, the
information (patient name, date of birth, etc.) will appear.
If analysis ordering is performed, the settings of the registered analysis order are
given priority.
[Query to Host] Specify whether or not the host computer is queried for the analysis order.
Select this checkbox to query the host.
Remove the checkmark when analyzing a sample without a registered analysis
order, such as a STAT sample.
[Aspiration Sensor] Specify whether or not the aspiration sensor is used.
Select the checkbox to use the aspiration sensor.
When the volume of blood to be aspirated is low, remove this checkmark.
[Cap Open] Select this checkbox to perform micro sample analysis (analysis with the sample
tube cap open).
[Raised Bottom Tube] Select the checkbox to use an RBT micro collection tube.
[Dispense] Use to prepare diluted blood.
Touch to start dispensing CELLPACK DCL. For the dispensing procedure, see the
following.
(➤P.148 "4.8.1 Preparing diluted blood with the diluent dispensing function (XN-530)")
Note:
• The instrument is equipped with an aspiration sensor. However, there is a possibility that correct results
may not be obtained if the sample volume is low and the sensor is not able to detect blood aspiration
error.
• If you know in advance that the blood sample is extremely thin, such as blood from a dialysis patient,
disable the aspiration sensor. For details, see Chapter 7.
(➤P.250 "Chapter 7: 7.9.1 Aspiration sensor settings")
8 Touch [OK].
The dialog box closes.
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11 If you are performing micro sample analysis (open analysis) with a regular
sample tube, or are performing analysis with a micro collection tube, remove
the sample tube cap.
When removing the cap, take care that the sample does not spill.
Caution!
If you are using an RBT micro collection tube, be sure to select the [Raised Bottom Tube] checkbox in step
7.
Otherwise there is a risk of instrument damage.
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Information
If a message appears during analysis prompting you to replace a reagent, replace the reagent. If the
reagent is replaced when the reagent is low, bubbling may occur and raise the blank value.
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Caution!
• The instrument does not mix the sample. Be sure to perform mixing immediately before starting analysis.
• Analysis cannot be performed in [Pre-Dilution] mode or [Body Fluid] mode when an RBT micro collection
tube is used.
2 If the sample tube holder is not ejected, press the sample tube holder
open/close switch.
The sample tube holder is ejected.
3 If you want to change the analysis mode, touch [Mode] in the control menu.
The [Change Measurement Mode] dialog box appears.
The analysis modes that appear depend on your system
configuration.
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5 Touch [OK].
The dialog box closes.
Checked
Background limits Remarks
parameter
WBC-BF 0.001 x 103/μL or White blood cell counts in body fluid measured from the
less WDF channel
RBC-BF 0.003 x 106/μL or Red blood cell counts in body fluid measured from the
less RBC/PLT channel
If the results are not within the allowable range after 3 analyses, a background check error occurs. See
"Troubleshooting". (➤Troubleshooting, "Chapter 1: 1.1 Error message list (in alphabetical order)")
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Note:
If the sample number is set to [Automatically increment Sample No. (manual mode)] and the analysis
settings are the same as the previously analyzed sample, settings of this dialog box can be omitted. For
details on auto increment of sample numbers, see Chapter 7.
(➤P.241 "Chapter 7: 7.8.4 Sample number auto increment settings")
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[Patient Information] Touch [Input] to enter the patient ID with the software keyboard.
If the patient information of the entered patient ID is registered in the instrument, the
information (patient name, date of birth, etc.) will appear.
If analysis ordering is performed, the settings of the registered analysis order are
given priority.
[Query to Host] Specify whether or not the host computer is queried for the analysis order.
Select this checkbox to query the host.
Remove the checkmark when analyzing a sample without a registered analysis
order, such as a STAT sample.
[Aspiration Sensor] Specify whether or not the aspiration sensor is used.
Select the checkbox to use the aspiration sensor.
When the volume of blood to be aspirated is low, remove this checkmark.
[Cap Open] Select this checkbox to perform micro sample analysis (analysis with the sample
tube cap open).
[Raised Bottom Tube] Select the checkbox to use an RBT micro collection tube.
[Dispense] Use to prepare diluted blood.
Touch to start dispensing CELLPACK DCL. For the dispensing procedure, see the
following.
(➤P.152 "4.8.2 Preparing diluted blood with the diluent dispensing function (XN-430)")
Note:
• The instrument is equipped with an aspiration sensor. However, there is a possibility that correct results
may not be obtained if the sample volume is low and the sensor is not able to detect blood aspiration
error.
• If you know in advance that the blood sample is extremely thin, such as blood from a dialysis patient,
disable the aspiration sensor. For details, see Chapter 7.
(➤P.250 "Chapter 7: 7.9.1 Aspiration sensor settings")
8 Touch [OK].
The dialog box closes.
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10 If you are performing micro sample analysis (open analysis) with a regular
sample tube, or are performing analysis with a micro collection tube, remove
the sample tube cap.
When removing the cap, take care that the sample does not spill.
Caution!
If you are using an RBT micro collection tube, be sure to select the [Raised Bottom Tube] checkbox in step
7.
Otherwise there is a risk of instrument damage.
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Information
If a message appears during analysis prompting you to replace a reagent, replace the reagent. If the
reagent is replaced when the reagent is low, bubbling may occur and raise the blank value.
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Caution!
The instrument does not mix the sample. Be sure to perform mixing immediately before starting analysis.
2 If you want to change the analysis mode, touch [Mode] in the control menu.
The [Change Measurement Mode] dialog box appears.
The analysis modes that appear depend on your system
configuration.
4 Touch [OK].
The dialog box closes.
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Checked
Background limits Remarks
parameter
WBC-BF 0.001 x 103/μL or White blood cell counts in body fluid calculated from the
less WDF channel
RBC-BF 0.003 x 106/μL or Red blood cell counts in body fluid calculated from the
less RBC/PLT channel
If the results are not within the allowable range after 3 analyses, a background check error occurs. See
"Troubleshooting". (➤Troubleshooting, "Chapter 1: 1.1 Error message list (in alphabetical order)")
Note:
If the sample number is set to [Automatically increment Sample No. (manual mode)] and the analysis
settings are the same as the previously analyzed sample, settings of this dialog box can be omitted. For
details on auto increment of sample numbers, see Chapter 7.
(➤P.241 "Chapter 7: 7.8.4 Sample number auto increment settings")
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Note:
• The instrument is equipped with an aspiration sensor. However, there is a possibility that correct results
may not be obtained if the sample volume is low and the sensor is not able to detect blood aspiration
error.
• If you know in advance that the blood sample is extremely thin, such as blood from a dialysis patient,
disable the aspiration sensor. For details, see Chapter 7.
(➤P.250 "Chapter 7: 7.9.1 Aspiration sensor settings")
7 Touch [OK].
The dialog box closes.
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10 Insert the pipette all the way to the bottom of the sample tube, and press the
start switch.
A beep sounds and sample aspiration starts. Analysis status indicator LED
The analysis status indicator LED blinks green during sample
aspiration. When aspiration ends, the instrument sounds two beeps
and the analysis status indicator LED turns OFF.
Information
If a message appears during analysis prompting you to replace a reagent, replace the reagent. If the
reagent is replaced when the reagent is low, bubbling may occur and raise the blank value.
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When the instrument is ready to analyze the next sample, a beep sounds and the analysis status indicator LED
lights green.
Caution!
After the sample is aspirated, remove the sample tube straight down so that it does not hit the pipette.
Otherwise correct analysis results may not be obtained or the sample may spill.
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1 Make sure the button on the right edge of the control menu is [Manual]. When
the mode is set to [Sampler], press the mode switch.
The mode changes to manual analysis mode.
Note:
If the mode switch is pressed while analysis is in progress in sampler analysis mode, sampler analysis will
pause when analysis of the current sample is completed, and the mode will change to manual analysis
mode.
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4 Touch [Pre-Dilution].
When changing to [Pre-Dilution] mode, the mode change will take time. Wait until the mode change is completed.
5 Touch [OK].
The dialog box closes.
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7 Touch [Dispense].
The instrument prepares for diluent dispensing, and when it
completes preparations, the dialog box on the right appears.
10 Place the empty micro collection tube in the sample tube holder.
Micro collection tube holder
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13 Touch [Cancel].
The diluent dispensing function finishes and the instrument
enters the analysis ready state. The dialog box on the right
appears during analysis preparation, and closes when
preparation finishes.
14 Dispense 20 μL of the sample into the micro collection tube containing the
diluent.
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2 If the sample tube holder is not ejected, press the sample tube holder
open/close switch.
The sample tube holder is ejected.
4 Touch [Pre-Dilution].
When changing to [Pre-Dilution] mode, the mode change will take time. Wait until the mode change is completed.
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5 Touch [OK].
The dialog box closes.
7 Touch [Dispense].
The instrument prepares for diluent dispensing, and when it
completes preparations, the dialog box on the right appears.
9 Place the empty micro collection tube in the sample tube holder.
Micro collection
tube holder
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12 Touch [Cancel].
The diluent dispensing function finishes and the instrument
enters the analysis ready state. The dialog box on the right
appears during analysis preparation, and closes when
preparation finishes.
13 Dispense 20 μL of the sample into the micro collection tube containing the
diluent.
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3 Touch [Pre-Dilution].
When changing to [Pre-Dilution] mode, the mode change will take time. Wait until the mode change is
completed.
4 Touch [OK].
The dialog box closes.
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6 Touch [Dispense].
The instrument prepares for diluent dispensing, and when it
completes preparations, the dialog box on the right appears.
8 Insert the pipette until it contacts the bottom of the micro collection tube, and
press the start switch.
Diluent dispensing starts. Analysis status indicator LED
While dispensing, keep the pipette in contact with the
bottom of the micro collection tube.
While diluent is dispensed, the analysis status indicator Pipette
LED blinks green and the beeper sounds repeatedly.
When dispensing finishes, the analysis status indicator
LED turns OFF and the beeping stops.
Micro collection
tube
Start switch
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Caution!
After dispensing the diluent, remove the micro collection tube straight down so that it does not hit the pipette.
Otherwise correct analysis results may not be obtained or the sample may spill.
10 Touch [Cancel].
The diluent dispensing function finishes and the instrument
enters the analysis ready state. The dialog box on the right
appears during analysis preparation, and closes when
preparation finishes.
11 Dispense 20 μL of the sample into the micro collection tube containing the
diluent.
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Chapter 5 Checking Analysis Results (Sample Explorer)
No
No
No
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Note:
Up to 100,000 analysis results can be saved. Once 100,000 results are saved, each new result
automatically deletes the result with the oldest analysis date and time.
Information
Flags (IP messages) are only intended for use in the clinical laboratory and are not for patient diagnosis.
Flags notify the operator of the possibility of a specific sample abnormality that requires examination of the
analysis results.
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Note:
You cannot search for a sample when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
[Sample No.] Up to 22 characters can be entered for the condition. Double-byte characters cannot
be entered.
[Patient ID] Up to 16 characters can be entered for the condition. Double-byte characters cannot
be entered.
[Last Name] (the Up to 20 characters can be entered for the condition.
patient's last name)
[First Name] (the Up to 20 characters can be entered for the condition.
patient's first name)
[Ward Name] Up to 20 characters can be entered for the condition.
[Doctor Name] Up to 20 characters can be entered for the condition.
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Note:
You can enter "?" and "∗" as wildcard characters in your search.
"?": Used as a wildcard for 1 character.
Example: If you search for "99?99", "99099", "99999", and "99A99" are all selected.
"∗": Used as a wildcard for 0 or more characters.
Example: If you search for "9∗9", "909", "9119", and "99A99" are all selected.
[PREV.] Touch to search upward from the analysis result selected in the list.
[NEXT] Touch to search downward from the analysis result selected in the list.
Note:
Touch [Condition] to return to the dialog box that shows the condition.
4 Touch [Close].
The dialog box closes.
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Multiple selection
mode button
[Sample Explorer] screen (Regular display)
If you want to perform an operation using the analysis results of multiple samples, change the mode of the analysis
result list to multiple selection mode.
Touch the multiple selection mode button to change to the multiple selection mode display below.
Enter marks to specify the analysis results you want to select.
Mark displays
Select button
Multiple selection
mode button
[Sample Explorer] screen (Multiple selection mode display)
Mark displays Analysis results that are marked (orange) will be the target of the operation.
Select button Touch to add marks to the analysis results on the line where the cursor is positioned.
If a mark already appears, the mark is cleared.
Select all button Touch to add a mark to all analysis results.
Cancel select all button Touch to clear the marks from all analysis results.
Multiple selection Touch to change the analysis result list to the regular display.
mode button
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Note:
• You cannot validate analysis results when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
• You can also set validation to be performed automatically. See Chapter 7.
(➤P.241 "Chapter 7: 7.8.5 Auto validate settings")
Follow the steps below to validate analysis results. This procedure is also used to cancel validation.
1 Select the analysis results you want to validate in the analysis result list.
If you want to perform an operation using the analysis results of multiple samples, change the mode of the
analysis result list to multiple selection mode and add marks. For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
If the analysis result list is in multiple selection mode and the analysis results of multiple samples are selected,
all selected analysis results change to the same validation state as the results where the cursor is positioned.
Note:
After validating, the sample number or other sample information cannot be changed. If you need to change
any information, cancel validation.
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Note:
• In the cases below, the analysis results cannot be output.
• The sample has not been validated.
• The last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
• The instrument is not connected to a host computer or printer.
• You can also set auto output to a host computer or graphic printer. See Chapter 7. (➤P.243 "Chapter 7:
7.8.6 Auto output settings")
1 Select the analysis results you want to output in the analysis result list.
If you want to perform an operation using the analysis results of multiple samples, change the mode of the
analysis result list to multiple selection mode and add marks. For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
2 Touch the output destination from the [Output] button on the toolbar.
Destinations that are not connected are grayed out and cannot be selected.
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Note:
• CSV output is not possible when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
• Note the following points when performing CSV output.
• The order of the output items cannot be changed.
• Scattergrams and distributions are separately output to an image file*.
Follow the steps below to save the analysis results in CSV format.
USB memory
stick
USB port
2 Select the analysis results you want to save in CSV format in the analysis
result list.
If you want to perform an operation using the analysis results of multiple samples, change the mode of the
analysis result list to multiple selection mode and add marks. For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
Note:
If you selected multiple analysis results for output, the results will be output in order from the top of list.
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• Image file
Instrument ID_Software version_Analysis date_Analysis time_Sample number_Image name.png (or bmp)
Example: XN-XXX_00-01_20140505_080808_1234_RBC.png
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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Note:
• You cannot back up data when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
• Whether or not the backup data includes patient information depends on the security settings. For details
on security, see Chapter 7.
(➤P.251 "Chapter 7: 7.9.3 Security settings")
USB memory
stick
USB port
2 Select the analysis results you want to save in the analysis result list.
If you want to perform an operation using the analysis results of multiple samples, change the mode of the
analysis result list to multiple selection mode and add marks. For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
Note:
If you selected analysis results of multiple samples, all selected analysis results are backed up to multiple
files.
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* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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Note:
You cannot restore analysis results when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
USB memory
stick
USB port
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4 Touch [OK].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the analysis result restore is complete.
Note:
If the logged on user does not have [Display and Modify Patient Info.] permission, a dialog box appears to
warn the user that patient information cannot be restored. To restore the data except for patient
information, touch [OK]. For details on [Display and Modify Patient Info.] permission, see Chapter 7.
(➤P.234 "Chapter 7: 7.8.1 User information management (user registration)")
• To change (overwrite) the registered patient information to the patient information in the backup file:
Select [Overwrite] and touch [Yes].
• To register the patient information in the backup file using a different ID:
Select [Register in different ID], enter the new patient ID in the entry field on the right, and touch [Yes].
Up to 16 characters can be entered for the patient ID. Double-byte characters cannot be entered.
• To restore analysis results without the patient information in the backup file:
Touch [No].
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Note:
Sample information cannot be modified in the following cases.
• The sample has been validated.
• The last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
1 Select the samples (analysis results) you want to modify in the analysis result list.
[Sample No.] Displays the sample number. To modify the sample number, it must be entered.
Up to 22 characters can be entered. Double-byte characters cannot be entered.
[Sample Inf.] Displays the sample number information. Select from [Manual Setting (M)], [Auto
Increment (A)], [ID Barcode Reader (B)], and [Host Setting (C)].
[Patient ID]* Displays the ID of the patient.
Up to 16 characters can be entered. Double-byte characters cannot be entered.
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4 Touch [OK].
The modified sample information is saved.
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Note:
You cannot delete analysis results when the last 10 samples are displayed using [Display].
For details on [Display], see the following.
(➤P.181 "5.11.3 Changing the display method of the analysis result list (display settings)")
1 Select the analysis results you want to delete in the analysis result list.
If you want to perform an operation using the analysis results of multiple samples, change the mode of the
analysis result list to multiple selection mode and add marks. For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
3 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
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Information
Flags (IP messages) are only intended for use in the clinical laboratory and are not for patient diagnosis.
Flags notify the operator of the possibility of a specific sample abnormality that requires examination of the
analysis results.
Toolbar
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[File] Touch to open a submenu that allows you to save and restore an analysis result.
[Output in CSV Format]: Use to save the analysis result in CSV format.
(➤P.166 "5.6 Saving analysis results in CSV format")
[Backup]: Use to back up the analysis result.
(➤P.168 "5.7 Saving analysis results (backup)")
[Restore]: Use to restore the backed up data.
(➤P.170 "5.8 Restoring saved analysis results
(restore)")
[Delete] Use to delete the data selected in the analysis result list.
(➤P.174 "5.10 Deleting analysis results")
Analysis result list Displays a list of the analysis results.
For details, see the following.
(➤P.177 "● Items that appear in the Sample Information tab")
(➤P.179 "● Items that appear in the Whole Blood Measurement tab")
(➤P.179 "● Items that appear in the Body Fluid Measurement tab")
(➤P.179 "● Items that appear in the Patient Information tab")
(➤P.180 "● Items that appear in the Reagent tab")
Tabs Touch to change the items displayed in the analysis result list.
: Reagent tab
The Body Fluid Measurement tab does not appear when the instrument does not
have the body fluid analysis function.
Multiple selection Touch to change the analysis result list to the multiple selection mode.
mode button For the multiple selection mode, see the following.
(➤P.163 "5.3 Selecting analysis results to validate/output")
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Displayed item
WBC-BF, RBC-BF, MN#, PMN#, MN%, PMN%, TC-BF#
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Data masks
Marks*1,2
*1 Only 1 mark can be shown per data. If an analysis result has multiple abnormalities, the abnormality that has
the highest priority is indicated. The order of priority is the same as the order of appearance of the marks in
the above table ([ ∗ ] has the highest priority).
*2 The priority levels of [ ∗ ] and [@] are changed in the service settings.
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[No Display Settings] Touch to change to the standard display method (sort conditions: date and time of
analysis in descending order, filter conditions: none).
[Last 10 Samples] Touch to change to the display of only the last 10 samples by the standard display method.
[Display Settings 1] to Touch to change to the sort conditions and filter conditions set in the corresponding
[Display Settings 3] item.
[Setting] Touch to set the sort conditions and filter conditions.
The name of the selected display method appears next to the screen name in the upper left corner of the screen.
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6 Touch [Regist.].
The dialog box closes and the set information is registered. The list display changes according to the set
conditions.
Note:
If analysis data is selected with display conditions specified and a condition is no longer satisfied due to the
date being changed or other reason, the selected state cannot be maintained. A dialog box appears to
notify you of the change of selection range.
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No
No
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1 In the [Sample Explorer] screen, select the analysis results for which you
want to check details.
3 Touch tabs.
The screen of the selected tab appears.
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Note:
When the [Data Browser] icon in the [Menu] screen is touched, the analysis results displayed in the [Data
Browser] screen changes according to the [Display] of the [Sample Explorer] screen.
• When set to [Last 10 Samples]
The latest analysis results appear.
• When set to other than [Last 10 Samples]
The analysis results selected in the [Sample Explorer] screen appear.
For details on [Display] in the [Sample Explorer] screen, see Chapter 5.
(➤P.181 "Chapter 5: 5.11.3 Changing the display method of the analysis result list (display settings)")
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Information
IP messages are only intended for use in the clinical laboratory and are not for patient diagnosis. Flags
notify the operator of the possibility of a specific sample abnormality that requires examination of the
analysis results.
Analysis results
* Does not appear when the instrument does not have the RET analysis function.
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When there is a rule comment, the comment icon appears on the right.
* The judgment results are only for use in the clinical laboratory. They are not intended for patient diagnosis.
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: Diluted sample
: Body fluid
When body fluid analysis is performed without clearing [Analysis result is
high], [BF] appears in white characters on a red background and body fluid
icon appears darker.
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Sample number
Sample comment
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Patient comment
If the logged on user does not have [Display and Modify Patient Info.] permission, only the patient category icon
appears.
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Distribution 1
Distribution 2
Scattergram 1 Scattergram 2
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Information
The analysis results below are not shown.
• Body fluid analysis
• Analysis error
• [Patient ID] is not registered
If there are multiple analysis results with the same reception date, only the analysis results of the sample
with the most recent analysis date and time are displayed.
There are 3 methods for displaying the [Cumulative] tab. The method can be changed in the submenu of the
[Switch] button on the toolbar.
Analysis date
Analysis date Displays the dates and times when the analysis results were made available.
Analysis items* Displays the analysis items.
Analysis results* Displays the analysis item data as numerical values.
* Research parameters are displayed on a gray background.
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Analysis date
Analysis date Displays the dates and times when the analysis results were made available.
Analysis items* Displays the analysis items.
Analysis results* Displays the analysis item data as broken-line graphs.
The right side of each graph shows the maximum value and minimum value of the
past 5 analysis results.
* Research parameters are displayed on a gray background.
Analysis date
Analysis date Displays the dates and times when the analysis results were made available.
Analysis items Displays the analysis items.
Analysis results Displays the analysis results of items as scattergrams and distributions.
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IP message
Grade value
Q-Flag
Trigger level
Positive if on or to right of this line
Negative if to left of this line
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Grade value This shows the Q-Flag result converted to a numerical value from 0 to 300 in
increments of 10. When it is greater than or equal to the trigger level (threshold value
for Positive), the result is Positive.
In addition, the following may appear in the judgment value position. Nothing is
displayed on the bar graph.
[Discrete]: The parameter used for judgment has not been analyzed (appears in gray).
[Error]: Judgment not possible.
Blank: Prerequisite for judgment not met or suspect judgment not performed
due to blank data or otherwise.
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Setting categories
Setting categories Touch an icon to display the setting dialog box of the category.
[Back] Touch to return to the [Menu] screen.
Note:
Settings cannot be configured while the instrument is in operation. Analysis cannot be started while
settings are being configured.
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Setting items
Setting area
5 Touch [OK].
Your setting changes are saved and the dialog box closes.
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[Output]
[Ledger (LP)] Touch to print the settings to the list printer.
(➤P.206 "7.3.1 Printing settings")
[File]
[Backup ALL Touch to back up the settings files.
Settings Files] (➤P.207 "7.3.2 Saving settings (backup)")
[Restore ALL Touch to change the current settings to the settings in the backup settings files.
Settings Files]* (➤P.208 "7.3.3 Restoring backed up settings (restore)")
[Initialize ALL Touch to initialize the settings to the factory settings.
Settings Files]* (➤P.210 "7.3.4 Initializing settings")
1 Touch the [Output] button on the toolbar in the [Setting] menu screen.
The submenu on the right appears.
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USB memory
stick
USB port
2 Touch the [File] button on the toolbar in the [Setting] menu screen.
The submenu on the right appears.
* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
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1 Insert the USB memory stick that contains the settings file.
Insert the USB memory stick into a free USB port on
the back of the instrument.
A USB memory stick with a password lock function
cannot be used.
USB memory
stick
USB port
2 Touch the [File] button on the toolbar in the [Setting] menu screen.
The submenu on the right appears.
4 Touch [Yes].
If there is only one setting file in the USB memory stick, the restore starts and the [Waiting to complete
execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the restore is complete.
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2 Touch [OK].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the restore is complete.
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1 Touch the [File] button on the toolbar in the [Setting] menu screen.
The submenu on the right appears.
3 Touch [Yes].
The settings are initialized.
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[System Language] Touch to set the language that appears on the screen and the language used for
printing.
(➤P.212 "7.4.1 Changing the display language (system language)")
[General Date Format] Touch to set the format of the date that is displayed and printed.
(➤P.212 "7.4.2 Date format settings")
[Patient ID Display Touch to set how the patient ID is displayed.
Settings] (➤P.213 "7.4.3 Patient ID display settings")
[Instrument Name Touch to set the instrument name.
Setting] (➤P.213 "7.4.4 Instrument name settings")
[Facility Information] Touch to set the name of the facility that is using the system.
(➤P.213 "7.4.5 Facility information settings")
[Scattergram Touch to set the background color of scattergrams.
settings] (➤P.214 "7.4.6 Scattergram settings")
[Set date] Touch to set the date and time of the system.
(➤P.214 "7.4.7 Date and time settings")
[Close] The dialog box closes.
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Note:
Changed settings will be applied the next time startup or logon is performed.
[General Date Format] The date format shown on the screen and used for
printing can be changed.
Select from the following.
[YYYY/MM/DD]: Year 4 digits/Month 2 digits/
Day 2 digits
[MM/DD/YYYY]: Month 2 digits/Day 2 digits/
Year 4 digits
[DD/MM/YYYY]: Day 2 digits/Month 2 digits/
Year 4 digits
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[Patient ID Display
Settings] dialog box
Note:
The patient ID displayed in the patient information area is always left-justified, regardless of the settings.
[Instrument Name
Setting] dialog box
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[Host Set whether or not the instrument is connected to the host computer.
Computer] If connected, set the communication method.
(➤P.216 "7.5.1 Host computer connection")
[Printer] Set whether or not the instrument is connected to a printer.
(➤P.218 "7.5.2 Printer connection")
[CSV Output] Specify whether image data is output when analysis results are output in CSV
format.
If output, set the output format and background color.
(➤P.218 "7.5.3 CSV output settings")
[Close] The dialog box closes.
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Communication
method
Settings
[Connect to Host Select this checkbox to enable connection to the host computer.
Computer] This must be selected to configure connection settings.
Communication Select [Serial Connection] or [TCP/IP Connection] for the method of communication
method with the host computer.
Settings Displays the detailed settings for the selected communication method.
[Modify Settings] Use to configure detailed settings for the selected communication method.
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[Format] Select [XN-L series Sysmex Standard] or [XN-L series ASTM] for the communication
format*.
When [XN-L series ASTM] is selected, the class cannot be selected.
[Port Setting] Select the port used for the connection.
[Baud Rate] Select the transmission speed.
[Code] Select the data bit length.
[Stop Bit] Select the stop bit length.
[Parity Bit] Select the parity check method.
[Interval] Select the transmission interval.
[Class] Select the transmission method.
* To use a format other than the above, service settings are required.
[Format] Select [XN-L series Sysmex Standard] or [XN-L series ASTM] for the communication
format*.
[Host IP Address] Set the IP address of the host computer.
[Port No.] Set the port number of the host computer.
Touch [-] to decrease the value. Touch [+] to increase the value.
* To use a format other than the above, service settings are required.
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Category list
Note:
If there is no information on the age or sex, or there is no applicable category, the limit values of the
universal category are automatically used.
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Reference
interval value list
[Specify Patient Select the patient category whose settings are to be configured.
Category] The settings of the selected category appear on the right.
(➤P.220 "7.6.1 Patient category settings")
Reference interval Displays a list of the reference interval values of the selected category.
value list When an item is selected, the settings appear on the right. The settings can be
changed.
[Lower Limit]*, Enter a value to set the lower limit and the upper limit for abnormal judgments.
[Upper Limit]* If a reference interval value is not needed, set the lower limit to [0] and the upper limit
to a high value such as 999.9.
* The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
• When the analysis value of a parameter exceeds the reference Interval, "+" or "-" appears on the right of
the data.
• Units cannot be set in this dialog box. To set the units, see the following. (➤P.239 "7.8.2 Unit settings")
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Critical value list Displays a list of the critical values (upper and lower limit values of analysis
parameters).
When an item is selected, the settings appear on the right. The settings can be
changed.
[Lower Limit]*, Enter a value to set the upper limit and the lower limit for analysis items.
[Upper Limit]*
* The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
• When the analysis value of a parameter exceeds the critical value, " ! " appears next to the data.
• Sampler analysis can be set to stop when there is data with " ! ". (XN-530)
• Units cannot be set in this dialog box. To set the units, see the following.
(➤P.239 "7.8.2 Unit settings")
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Flag list
Judgment
conditions
Flag list Displays a list of the flags and the set judgment conditions.
When a flag is selected, the settings appear at the bottom. The settings can be
changed.
[Judge] Select this checkbox to enable the selected flag judgment.
*
Judgment conditions Enter a value for the judgment conditions.
* The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
For details on flags and the values that can be entered, see "Troubleshooting".
(➤Troubleshooting, "Chapter 5: 5.3 IP message judgment conditions and judgment methods")
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Flag list
Judgment
conditions
Flag list*1 Displays a list of the flags and the set judgment conditions.
When a flag is selected, the settings appear at the bottom. The settings can be
changed.
[Judge] Select this checkbox to enable the selected flag judgment.
Judgment Enter a value for the judgment conditions.
conditions*2
*1 [Reticulocytosis] does not appear when the instrument does not have the RET analysis function.
*2 The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
For details on flags and the values that can be entered, see "Troubleshooting".
(➤Troubleshooting, "Chapter 5: 5.3 IP message judgment conditions and judgment methods")
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Flag list
Judgment
conditions
Flag list Displays a list of the flags and the set judgment conditions.
When a flag is selected, the settings appear at the bottom. The settings can be
changed.
[Judge] Select this checkbox to enable the selected flag judgment.
Judgment conditions* Enter a value for the judgment conditions.
* The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
For details on flags and the values that can be entered, see "Troubleshooting".
(➤Troubleshooting, "Chapter 5: 5.3 IP message judgment conditions and judgment methods")
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Note:
This setting does not appear when the instrument does not have the body fluid analysis function.
Touch [WBC (Body Fluid Analysis) Flags] in the [Data analysis Setting] dialog box.
Flag list
Judgment
conditions
Flag list Displays a list of the flags and the set judgment conditions. (There is only 1 WBC
abnormal flag for body fluid analysis.)
[Judge] Select this checkbox to enable the flag judgment.
Judgment conditions* Enter a value for the judgment conditions.
* The XN-L series displays the decimal point symbol set in Windows.
The only decimal point symbols displayed are "." (period) and "," (comma).
Note:
For details on flags and the values that can be entered, see "Troubleshooting".
(➤Troubleshooting, "Chapter 5: 5.3 IP message judgment conditions and judgment methods")
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7.7 QC settings
To display the [QC Setting] dialog box, touch the [QC Setting] icon in the [Setting] menu screen.
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7.7.1 QC settings
Touch [QC Setting] in the [QC Setting] dialog box.
* [Number of RET Samples] does not appear when the instrument does not have the RET analysis function.
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Alarm select tabs Three alarms that prompt you to perform QC can be registered, and the settings of
each alarm are configured by selecting the tabs.
[Use] When selected, the alarm will sound.
[Time] Set the time when the alarm will sound.
Touch [-] to decrease the value. Touch [+] to increase the value.
[Repeating Day The alarm will sound on the selected days of the week.
Specification]
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QC chart fixed
comment list
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[QC Chart Screen] Specify whether or not the plotted data is automatically output to the host
computer when QC data is plotted on a QC chart.
[QC Files Select this checkbox to have plotted data (excluding X-barM control)
(Excluding X-barM)] automatically output to the host computer.
[X-barM Files] Select this checkbox to have X-barM control plotted data automatically output
to the host computer.
[Explorer Screen] Specify whether or not the analysis results of sample numbers that start with
"QC-" are automatically output.
[Graphic Printer (GP)] Select this checkbox to have the data output to the graphic printer.
[Host Computer (HC)] Select this checkbox to have the data output to the host computer.
Note:
To output data to the host computer, a connection to the host computer is required.
(➤P.216 "7.5.1 Host computer connection")
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[User Management] Register and delete users of the instrument. Auto logon can also be set.
(➤P.234 "7.8.1 User information management (user registration)")
[Unit] Set the units of analysis values. (➤P.239 "7.8.2 Unit settings")
[Alarm Sound Setting] Set the alarm sound that alerts you when an error has occurred.
(➤P.240 "7.8.3 Alarm sound settings")
[Sample No. Auto Specify whether sample numbers are automatically incremented.
Increment] (➤P.241 "7.8.4 Sample number auto increment settings")
[Auto Validate] Specify whether analysis results are automatically validated.
(➤P.241 "7.8.5 Auto validate settings")
[Auto Output] Specify whether analysis results are automatically output to the host computer or
graphic printer. (➤P.243 "7.8.6 Auto output settings")
[Analysis Ordering] Set the keys and method used to query the host computer for analysis information.
(➤P.245 "7.8.7 Analysis ordering settings")
[Delta Check] Specify whether delta check is performed.
(➤P.246 "7.8.8 Delta check settings")
[Sleep Setting] Set the time until the instrument enters the sleep state when left idle.
(➤P.247 "7.8.9 Sleep settings")
[Repeat Setting]* Specify whether Repeat analysis is performed.
(➤P.247 "7.8.10 Repeat settings (XN-530)")
[Rerun/Reflex Specify whether Rerun analysis and Reflex analysis are performed.
Setting]* (➤P.247 "7.8.11 Rerun/Reflex settings (XN-530)")
* XN-530 only.
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User list
[Auto Logon] To use auto logon, select the user (logon name) used for logon.
To not use auto logon, select [No].
User list Displays a list of the users.
To change user information or delete a user, select the user in the list and touch a
button at the bottom of the screen.
To change information or permissions: Select the user and touch [Modify].
To delete: Select the user and touch [Delete].
[Change Password] The password of the currently logged on user can be changed.
(➤P.235 "● Changing password")
[Modify]*1,2 User information and permissions can be changed.
(➤P.236 "● Changing settings and adding users")
[Add] A user can be added.
When the maximum number of users (100) have been registered, a user cannot be
added.
(➤P.236 "● Changing settings and adding users")
[Delete]*2 Use to delete a user selected in the user list.
(➤P.238 "● Deleting users")
*1 You can also double-click a user in the user list whose settings you want to change to open a dialog box.
*2 The [admin] (instrument administrator) cannot be deleted. Aside from the [admin] (instrument administrator)
password, nothing can be changed.
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● Changing password
Follow the steps below to change the password.
3 Touch [OK].
The password is changed.
Note:
A user with [All Administrators] permission and the [admin] (instrument administrator) can change the
passwords of other users with the [Modify] procedure. For details on changing settings, see the following.
(➤P.236 "● Changing settings and adding users")
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Note:
The maximum number of users that can be registered is 100.
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4 Touch [OK].
The dialog box closes and the settings are changed or the user is added.
● Deleting users
Follow the steps below to delete an user.
Note:
• Users with [All Administrators] permission and the [admin] (instrument administrator) can delete other
users.
• The [admin] (instrument administrator) cannot be deleted.
2 Touch [Delete].
The dialog box on the right appears.
3 Touch [Yes].
The deletion starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the deletion is complete.
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Unit list
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[Alarm for Analysis Set the alarm sound that alerts you when an analysis stop error has occurred.
Stop Error] [No Alarm]: No alarm sound.
[Once]: The alarm sounds once.
[Loop]: The alarm sounds repeatedly until the screen is touched.
Note:
The alarm sound settings for emergency stop errors such as an instrument failure cannot be changed.
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[Auto Validate] Select this checkbox to have the samples automatically validated.
[Auto Validate Setting Select the setting method for validate conditions.
Procedure] [Set in rule view]: Validate based on the conditions set on the
[Validation Rule] tab of the [Rule] screen.
[Use simple settings]: Validate based on the conditions set in the
dialog box that appears when [Modify Settings]
is touched.
[Settings] Displays the settings or the reference location for the selected auto validate
setting method.
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[All Samples] All samples will be automatically validated regardless of the analysis mode.
[Negative Sample] Automatically validate samples with [Negative] analysis results.
[Negative and Automatically validate samples with [Negative] analysis results and no error
Unmarked] marks.
[Negative and Delta Automatically validate samples with [Negative] analysis results and no delta
Check Negative]* check errors.
[Negative and Unmarked Automatically validate samples with [Negative] analysis results and no error
and Delta Check marks or delta check errors.
Negative]*
Note:
Only analysis results that have been validated can be output.
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[Auto Output] Select this checkbox to have validated samples automatically output.
[Auto Output Setting Select the setting method for auto output conditions.
Procedure] [Set in rule view]: Automatically output analysis results based on the
conditions set on the [Output Rule] tab of the [Rule]
screen.
[Use simple settings]: Automatically output analysis results based on the
conditions set in the dialog box that appears when
[Modify Settings] is touched.
[Settings] Displays the settings or the reference location for the selected auto output setting
method.
[Modify Settings] Use to configure detailed settings for [Use simple settings].
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[Do not automatically When this checkbox is selected, data that includes errors are not output to all output
output data with destinations, regardless of the output conditions.
errors]
[Auto Output Set the output destinations and the output conditions for each destination.
Destination and
Output Conditions]
[GP] Select this checkbox to have the data output to the graphic printer.
[HC] Select this checkbox to have the data output to the host computer.
[Negative Data] Select data that has no parameters judged abnormal and no analysis errors.
[Diff. Posi.] Select sample data with abnormal blood cell differentiation.
[Morph. Posi.] Select sample data with abnormal blood cell morphology.
[Count Posi.] Select sample data with abnormal blood cell counts.
Note:
Data which has already been transmitted will not be transmitted again, if auto output is selected.
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Note:
If you attempt to change [Key Setting] when there is a pending order in the [Work List] screen, a warning
dialog box will appear to inform you that this is not possible. Analyze or delete the pending order first and
then change the settings.
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● Delta check
Using the patient ID as a key, delta check compares the most recent analysis results with the previous analysis
results and judges if the data is abnormal based on any changes in the data.
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[Rerun/Reflex Setting]
dialog box
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[Enable password Select this checkbox to enable the password character restriction.
character restriction] When enabled, passwords must be at least 6 characters, and must be a combination
of upper and lower case letters and numbers.
[Description]: Displays a detailed description.
[Enable password Select this checkbox to set the password expiration restriction.
expiration restriction] [Description]: Displays a detailed description.
[Expiration period] Set the password expiration date.
This can be set from 1 to 999 days.
[Prior notification of Set the date for sending notification prior to password expiration.
password expiration] If notification is not required, enter the same date as in [Expiration period].
This can be set from 1 to 999 days.
[Enable password- Select this checkbox to cause password changes to be remembered so that
reuse restriction] previously used passwords cannot be used again.
[Description]: Displays a detailed description.
[Password history] Set the number of passwords to be remembered.
This can be set from 1 to 99 passwords.
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[Aspiration Sensor]
dialog box
Caution!
Not using the [Aspiration Sensor] may affect analysis results. For [Whole Blood] mode analysis, select
[Use].
Note:
• If you know in advance that the blood sample is extremely thin, such as blood from a dialysis patient,
disable [Aspiration Sensor].
• The aspiration sensor is not used in pre-dilution mode and body fluid analysis, regardless of this setting.
Caution!
Unless otherwise directed by your local Sysmex representative, keep the setting set to OFF. If continuously
used with the setting set to ON, the instrument and other devices may be damaged if a leak occurs.
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[Include patient Select this checkbox to include patient information when analysis results backup.
information]
[Output patient Select this checkbox to include patient information, ward names, and doctor names
information] when outputting analysis results to a CSV file. CSV output of patient information,
ward names, and doctor names will also be possible.
[Use IPU screen lock Select this checkbox to turn ON the screen lock timer.
timer] When the instrument is left idle for the time set on the timer, the screen locks and
cannot be used.
[Time until IPU Set the time until the screen is locked by the screen lock timer. The time can be set
screen lock] from 15 to 60 minutes in increments of 1 minute.
Touch [-] to decrease the value. Touch [+] to increase the value.
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[Read Tube ID] Select this checkbox to turn ON the barcode reader.
[Specify Sample No. Select the number of digits that are read.
Length] To not specify a number of digits, select [No].
If a number of digits other than the specified number is read, a read error will occur.
However, sample numbers reserved in the system for quality control ([QC-]) and
rinsing ([RN-]) are not subject to the digit number check.
[Setting for Order Key Specify whether or not a sample for which an order key read error occurs is
Read Error] analyzed.
When this checkbox is selected, analysis is performed using the default analysis
information specified at the start of sampler analysis. When not selected, a sample
for which an order key read error occurs is not analyzed.
When ID read error is specified as a sampler stop condition, the sample is analyzed
or skipped based on this setting after operation is resumed.
[Check Digits Set the barcode specifications.
Conditions]
[ITF] Select this checkbox to enable reading of ITF barcodes.
Select [Modulus-10] or [Through] for the check digit.
[NW7] Select this checkbox to enable reading of CODABAR/NW7 barcodes.
Select [Modulus-11], [W-Modulus-11], [Modulus-16], or [Through] for the check digit.
[CODE39] Select this checkbox to enable reading of CODE39 barcodes.
Select [Modulus-43] or [Through] for the check digit.
[JAN] Select this checkbox to enable reading of JAN/EAN/UPC barcodes.
The check digit is fixed at Modulus-10.
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[ID Read Error] Select this checkbox to have sampler analysis stop when a sample tube barcode
label cannot be read.
[Blank Data] Select this checkbox to have sampler analysis stop when the count is extremely low.
[Critical Value Data] Select this checkbox to have sampler analysis stop when the critical value is
exceeded.
(➤P.222 "7.6.3 Critical value settings")
[Aspiration Error] Select this checkbox to have sampler analysis stop when blood cannot be aspirated
or an insufficient volume is aspirated.
This can be set when the aspiration sensor is used.
(➤P.250 "7.9.1 Aspiration sensor settings")
[QC Alarm] Select this checkbox to have sampler analysis stop when the QC alarm sounds.
This can be set when the QC alarm is used.
(➤P.229 "7.7.2 QC alarm settings")
[X-barM Limit Error] Select this checkbox to have sampler analysis stop when an X-barM control error
occurs in QC.
[L-J Limit Error] Select this checkbox to have sampler analysis stop when an L-J or X-bar control
error occurs in QC.
[Control Select this checkbox to have sampler analysis stop when the control blood is past its
Expired Error] expiration date.
[Unregistered Select this checkbox to have sampler analysis stop when the control blood has not
Control] been registered.
[Reagent Expired Select this checkbox to have sampler analysis stop when the reagent is past its
Error] expiration date.
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Warning!
• Data output in lab format is for research purposes only. Do not use for the diagnosis of patients.
• When report format is displayed in the layout screen, parameters for research cannot be displayed in the
template.
• Analysis data
• Sample information
• Analysis parameter
• Reference interval
• Scattergram*1
• Distribution*1
• IP message
• Q-Flag*2
• QC chart
*1 Colors cannot be specified.
*2 Lab format only.
• Optional items
• Text
• Line
• Image (BMP, JPG, GIF, PNG)
• Table
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Item System
OS Windows 7 or Windows 10
CPU 1.6 GHz or more
Memory 2 GB or more
Monitor 1920 x 1080 or more
Hard disk capacity 32 GB or more
Runtime Windows 7
Microsoft .NET Framework 4.0
Windows 10
Microsoft .NET Framework 4.6.2
Port USB port*
* Used for exchange of data with the instrument.
USB memory
stick
USB port
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4 Remove the USB memory stick from the instrument and insert it into the
computer.
7 Double-click "GPCustomize.exe"*.
"GPCustomize.exe" is GP Customize Tool.
GP Customize Tool starts and the [GP Customize] screen appears.
9 When you have finished editing the format, click the [Save] button on the
toolbar.
The edited format is saved in the "GPCustomize" folder.
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12 Remove the USB memory stick from the computer and insert it into the
instrument.
14 Touch [Yes].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the layout file restore is complete.
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Common
Text and lines properties
Templates
Specific
properties
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Templates Sample information and analysis parameters are arranged in sets of names and
values. Frequently used combinations of edit items are pre-grouped in
templates.
Click the [New] button on the toolbar to open a dialog box for selecting the
template. A template can be selected from the list that appears in the dialog box.
To cancel a template, click the [Cancel Template] button on the toolbar. Table
edit items cannot be canceled. The size of a template cannot be changed.
[Sample Info] Click to set the sample information template.
[Analysis items] Click to set the analysis items template.
[Reference Click to set the reference interval template.
Interval]
[Scattergram] Click to set the scattergram template.
[Distribution] Click to set the distribution template.
[IP Message] Click to set the IP message template.
[Q-Flag] Click to set the Q-Flag template (report format only).
Layout screen The layout screen shows the print image.
The selected edit items and template appear in the layout.
The layout area is 196 x 259 mm. The print size is A4 (210 x 297 mm).
A dummy image will appear in the layout screen.
Tab The print format is changed using the tabs. Click a tab to select the print format.
[Report Format] Click to select a report format.
Sample information and reportable parameters are printed. Only validated data
can be printed.
Properties The properties of the edit item that is selected in the layout screen are
displayed. Details can be set for each item.
When an edit item is not selected in the layout screen, the properties do not
appear.
[Common Property] Detailed information common to all edit items is displayed.
The position of the X and Y coordinates is displayed based on the point at the
top left of the item.
[Name] Displays the edit item name. Immediately after an item is selected for editing,
the default name ("Item" + "Serial number") appears. This name can be
changed.
Up to 32 characters can be entered. Double-byte characters cannot be entered.
[X] The X coordinate of the item (excluding lines) is shown in the layout screen. This
can be entered within the range 0 to 555 pt.
[Y] The Y coordinate of the item (excluding lines) is shown in the layout screen. This
can be entered within the range 0 to 733 pt.
[Width] The width of the edit item (excluding lines) is shown.
This can be entered within a range up to 556 pt. The lower limit of the range
varies depending on the object.
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Note:
The default file name is as follows.
[Instrument ID][Software version].gpf
4 Click [Save].
The layout is saved.
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3 Click [Open].
The layout selected for the layout screen is displayed.
Screens displayed
Files to be restored
For report use For lab use
For report use ✓ ✓
For lab use ‒ ✓
● Initializing a layout
An edited layout can be initialized.
Follow the steps below to initialize a layout.
2 Click [Yes].
The layout screen is initialized.
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Information
If you want to change, register, delete, or copy rules, contact your Sysmex service representative.
Note:
The rules are not applied to the results of analysis for maintenance (QC), analysis of sample number "0",
and analysis that resulted in a barcode reader read error.
XN-430
Rules XN-530 Overview
XN-330
Repeat rule ✓ ‒ Repeat analysis is performed based on the rule
judgment of the analysis results.
Rerun/Reflex/ ✓ ‒ Rerun analysis or Reflex analysis is performed and
Comment rule* a comment is added based on the rule judgment of
the analysis results.
Comment rule* ‒ ✓ A comment is added based on the rule judgment of
the analysis results.
Validation rule* ✓ ✓ Validation is performed based on the rule judgment
of the analysis results.
Output rule* ✓ ✓ Output is performed based on the rule judgment of
the analysis results.
* Up to 100 rules can be set.
● Analysis
Repeat analysis: Repeats the first analysis.
Rerun analysis: Repeats analysis of the sample while holding the results of the first analysis.
Reflex analysis: Tests additional parameters due to the results of the first analysis.
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● Repeat rules
[Repeat] means to repeat the analysis if an error occurs in the first analysis.
If an error occurs in the first analysis, Repeat analysis is performed automatically. Repeat rule is set for each
error message. The setting can be checked in the [Repeat Rule] tab on the [Rule] screen.
(➤P.272 "● [Repeat Rule] tab")
The Repeat rule judgment is only performed when [Repeat Setting] is ON. For details, see the following.
(➤P.247 "7.8.10 Repeat settings (XN-530)")
* The error messages below are [BlockRepeat (Fixed)], and are not displayed in the [Repeat Rule] tab.
• [Pressure Sensor Error]
• [Vacuum Sensor Error]
• [Reagent heater thermistor error]
• [Environment temperature thermistor error]
• [FCM reaction chamber thermistor error]
• [FCM sheath thermistor error]
• [Insufficient blood volume (short sample)]
• [Blood cannot be aspirated.]
● Rerun/Reflex/Comment rules
The results of the first analysis are judged, and Rerun analysis, Reflex analysis, or addition of a comment is
automatically performed. The judgment conditions for Rerun analysis, Reflex analysis, and comments can be set.
Rerun/Reflex/Comment rules do not function if an error occurs in the first analysis.
Rerun/Reflex/Comment rule judgment is only performed when [Rerun/Reflex Setting] is ON. For details, see the
following.
(➤P.247 "7.8.11 Rerun/Reflex settings (XN-530)")
● Rerun
[Rerun] is used to judge the analysis results and automatically rerun the test.
The results of the first analysis are judged, and Rerun analysis is automatically performed. Set the
judgment conditions for performing Rerun analysis.
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● Reflex
[Reflex] is used to judge analysis results and automatically perform analysis with additional discrete items
not analyzed in the initial analysis.
The results of the first analysis are judged, and Reflex analysis is performed on parameters that were not
analyzed in the initial test. Set the judgment conditions for performing Reflex analysis of the initial analysis.
● Comment
The comment setting is used to judge the analysis results and automatically displays a comment.
If [None] is selected for the action, a conditional expression that only sets a comment can be set.
● Comment rules
The comment setting is used to judge the analysis results and automatically displays a comment.
If [None] is selected for the action, a conditional expression that only sets a comment can be set.
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● Validation rules
To validate means to approve the output of the analysis data for reporting. Set the validation rules with the
judgment conditions for automatically performing validation.
Analysis results that have been already judged by the Repeat rule or the Rerun/Reflex/Comment rule are
judged, and validation is automatically performed.
● Output rules
Set the output rule with the judgment conditions for automatically outputting analysis results.
Analysis results that have been validated are judged and automatically output. The output destination can also
be set.
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Rule list
Tabs*
[Rule] screen
* The tabs that appear vary depending on the instrument that is used.
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Note:
The Repeat rule is applied when an error occurs in the results of the first analysis, and when an error
occurs in the results of Rerun analysis or Reflex analysis. Repeat analysis is not possible for some errors.
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Rule setting area Displays whether the rule is ON ([ ]), OFF ([ ]), or invalid ([ ]).
[No.] Displays the rule number. If a number greater than "100" (the maximum number
that can be registered) is entered, the number is displayed in red.
[Name] Displays the name of the rule. If not entered, nothing appears.
[Action] Displays the following actions.
[None] Rerun analysis and Reflex analysis are not performed.
[BlockRerunReflex] Rerun analysis and Reflex analysis are not performed.
Even if there are other conditions with [Rerun] or [Reflex] set for the action that
are satisfied, if a condition with [BlockRerunReflex] set is satisfied,
[BlockRerunReflex] is given priority.
[Rerun] Rerun analysis is performed.
[Reflex] Reflex analysis is performed. The discrete item of the added channel appears in
the parentheses. Even when the judgment is [Reflex], if the analysis items
belong to the discretes to be added and all channels were analyzed in the initial
analysis, Reflex analysis will not be performed.
[QueryToHost]* The host computer is queried to determine if Rerun analysis and Reflex analysis
are necessary.
[Conditional Expression] Displays the conditional expression for Rerun analysis, Reflex analysis, or
addition of a comment.
[Action Comment] Displays the comment to be added to the analysis data. Nothing appears if no
comments have been entered. The display color varies as follows depending on
the importance of the comment.
[Low] Appears in black characters on a white background.
[Medium] Appears in black characters on an orange background.
[High] Appears in white characters on a red background.
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[Update Date] Displays the date and time the rule was registered or last modified.
[Description] Displays a description of the rule. If not entered, nothing appears.
Note:
The results of [Rerun] analysis or [Reflex] analysis cannot be consolidated with or compared to the results
of the first analysis.
Rule setting area Displays whether the rule is ON ([ ]), OFF ([ ]), or invalid ([ ]).
[No.] Displays the rule number. If a number greater than "100" (the maximum number that
can be registered) is entered, the number is displayed in red.
[Name] Displays the name of the rule. If not entered, nothing appears.
[Action Comment] Displays the comment to be added to the analysis data. Nothing appears if no
comments have been entered. The display color varies as follows depending on the
importance of the comment.
[Low] Appears in black characters on a white background.
[Medium] Appears in black characters on an orange background.
[High] Appears in white characters on a red background.
[Conditional Displays the conditional expression for addition of a comment.
Expression]
[Update Date] Displays the date and time the rule was registered or last modified.
[Description] Displays a description of the rule. If not entered, nothing appears.
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Rule setting area Displays whether the rule is ON ([ ]), OFF ([ ]), or invalid ([ ]).
[No.] Displays the rule number. If a number greater than "100" (the maximum number that
can be registered) is entered, the number is displayed in red.
[Name] Displays the name of the rule. If not entered, nothing appears.
[Action] Displays the following actions.
[BlockValidate] Validation is not performed. Even if there are other conditions with [Validate] set for
the action that are satisfied, if a condition with [BlockValidate] set is satisfied,
[BlockValidate] is given priority.
[Validate] Validation is performed.
[Conditional Expression] Displays the conditional expression that determines whether validation is performed.
[Update Date] Displays the date and time the rule was registered or last modified.
[Description] Displays a description of the rule. If not entered, nothing appears.
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Rule setting area Displays whether the rule is ON ([ ]), OFF ([ ]), or invalid ([ ]).
[No.] Displays the rule number. If a number greater than "100" (the maximum number that
can be registered) is entered, the number is displayed in red.
[Name] Displays the name of the rule. If not entered, nothing appears.
[Action] Displays the following actions.
[BlockReport] Data is not output. Even if there are other conditions with [ReportTo] set for the
action that are satisfied, if a condition with [BlockReport] set is satisfied,
[BlockReport] is given priority.
[ReportTo] Data that has been validated is output. The output destination appears in the
parentheses.
[Conditional Displays the conditional expression for output.
Expression]
[Update Date] Displays the date and time the rule was registered or last modified.
[Description] Displays a description of the rule. If not entered, nothing appears.
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1 Select the rule you want to enable or disable in the rule list.
*1 [Rerun/Reflex/Comment Rule], [Comment Rule], [Validation Rule], and [Output Rule] only.
*2 [Repeat Rule] only.
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Note:
The rules should be saved during initial setting of the instrument and whenever there are updates or changes.
USB memory
stick
USB port
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* If a folder with the instrument ID as the folder name does not exist in the USB memory stick, the folder is
automatically created.
USB memory
stick
USB port
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2 Touch [OK].
The [Restore] dialog box appears.
4 Touch [OK].
The dialog box on the right appears.
5 Touch [Yes].
The restore starts and the [Waiting to complete execution] dialog box appears.
The [Waiting to complete execution] dialog box closes when the rule restore is complete.
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Note:
Rule sorting settings and simple settings are retained even when rules are restored.
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3 Touch [OK].
The dialog box on the right appears.
4 Touch [Yes].
The rules are initialized.
Note:
Rule sorting settings and simple settings are retained even when the rules are initialized.
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Index
Index
A D
Alarm sound settings....................................... 240 Data analysis settings...................................... 219
Analysis method.............................................. 118 Data Browser................................................... 185
Analysis mode................................................. 119 [Cumulative] tab .......................................... 197
Analysis ordering settings ............................... 245 [Graph] tab .................................................. 196
Analysis registration .......................................... 28 [Main] tab .................................................... 195
Backup.......................................................... 36 [Q-Flag] tab ................................................. 199
Delete ........................................................... 32 Screens...............................................186, 188
Display settings............................................. 61 Date and time settings..................................... 214
Modify ........................................................... 31 Date format settings ........................................ 212
Output ........................................................... 35 Delta check settings ........................................ 246
Print .............................................................. 35 DIFF ................................................................ 119
Register ........................................................ 28 Diluent dispensing function (XN-330) .............. 155
Restore ......................................................... 37 Diluent dispensing function (XN-430) .............. 152
Screens......................................................... 60 Diluent dispensing function (XN-530) .............. 148
Search .......................................................... 33 Discrete ........................................................... 119
Aspiration sensor settings ............................... 250 Display and modify patient information............ 237
Auto output condition settings ......................... 243 Display and output of research items .............. 237
Auto validate settings ...................................... 241 Display settings ............................................... 211
Doctor name registration
B Backup .......................................................... 55
Background check............................................. 11 Delete............................................................ 53
Backup Display settings............................................. 71
Analysis registration...................................... 36 Functions ...................................................... 39
Doctor name registration .............................. 55 Modify ........................................................... 53
GP Customize............................................. 265 Output in CSV format.................................... 54
Patient information registration ..................... 55 Register......................................................... 51
QC files ....................................................... 102 Restore ......................................................... 57
Rules........................................................... 278 Screens......................................................... 70
Sample Explorer ......................................... 168 Search........................................................... 54
Settings....................................................... 207
Ward name registration ................................ 55 F
Barcode reader connection settings................ 252 Facility information settings ............................. 213
Basic operation ................................................... 7
Buttons common to multiple screens ................ 19 G
GP Customize ................................................. 255
C Backup ........................................................ 265
CBC................................................................. 119 Functions .................................................... 255
Changing the display language....................... 212 Initialize ....................................................... 266
Checking analysis results................................ 159 Restore ....................................................... 265
Operation flow............................................. 159 Screens....................................................... 259
Checking detailed analysis results .................. 185 Graphic printer print settings ........................... 255
Operation flow............................................. 185
Comment rules................................................ 269 H
Control menu..................................................... 21 Host computer connection settings ................. 216
Critical value settings ...................................... 222 Serial connection ........................................ 216
CSV output settings ........................................ 218 TCP/IP connection ...................................... 217
Cursor data ..................................................... 100
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Index
I P
Instrument name settings ................................213 Patient category settings..................................220
Instrument settings ................................. 201, 249 Patient ID display settings................................213
Patient information registration
L Backup...........................................................55
Leak sensor settings ........................................250 Delete ............................................................41
Logoff .................................................................16 Display settings .............................................65
Logon .................................................................10 Functions .......................................................39
Lot information Modify ............................................................41
Auto registration (XN-530).............................77 Output in CSV format ....................................44
Manual registration........................................78 Register .........................................................39
Modify............................................................99 Restore ..........................................................57
Reading assay file .................................. 77, 79 Screens .........................................................64
Search ...........................................................43
M PLT abnormal flag settings...............................225
Main screen .......................................................20 Preparation for analysis (registering
Managing the password...................................248 information) .....................................................27
Manuals .............................................................17 Operation flow ...............................................27
Menu Print
Data analysis settings .................................219 Analysis registration ......................................35
Display settings .................................... 25, 211 QC charts ......................................................97
Instrument settings ......................................249 Rules ...........................................................278
Item list ..........................................................26 Sample Explorer ..........................................165
Operational settings ....................................232 Settings........................................................206
Output settings ............................................215 Printer connection settings...............................218
QC settings..................................................227
Screens .........................................................23 Q
Multiple selection mode ............................ 32, 163 QC alarm settings ............................................229
QC chart data auto output settings ..................231
O QC chart fixed comment settings .....................230
Operation flow......................................................7 QC charts
Analysis registration ......................................27 Cursor data management ............................100
Checking analysis results............................159 Output to host computer ................................97
Checking detailed analysis results ..............185 Print ...............................................................97
Quality control (QC).......................................73 Range select..................................................95
Sample analysis ..........................................117 Screens ................................................ 93, 110
Operational settings .........................................232 Shift display .................................................115
Output in CSV format Sort ..............................................................114
Analysis results ...........................................166 Vial line ................................................... 94, 96
Doctor name registration ...............................54 QC files
Patient information registration......................44 Backup.........................................................102
Ward name registration .................................50 Delete ..........................................................101
Output rules .....................................................270 Display settings ...........................................107
Output settings.................................................215 Overview........................................................75
Overall flow of operation ......................................7 Restore ........................................................103
Screens .......................................................105
QC materials ......................................................74
QC settings ............................................. 227, 228
Q-Flag ..............................................................199
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Index
T
Turning OFF the power......................................12
Turning ON the power..........................................9
Inspection ........................................................8
U
Unit settings .....................................................239
User information
Add ..............................................................236
Changing password.....................................235
Changing settings........................................236
Delete ..........................................................238
Management ...............................................234
User permission ...............................................236
User registration ..............................................234
V
Validate ................................................... 164, 241
Validation rule ..................................................270
Version ...............................................................25
Vial line ....................................................... 94, 96
W
Ward name registration
Backup ..........................................................55
Delete ............................................................48
Display settings .............................................69
Functions.......................................................39
Modify............................................................47
Output in CSV format ....................................50
Register .........................................................45
Restore..........................................................57
Screens .........................................................68
Search ...........................................................49
WBC abnormal flag (body fluid analysis)
settings .........................................................226
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