Operator's Manual
Table Of Contents
- What is new in publication version 7.2?
- 1 Introduction
- 1.1 Before you start
- 1.2 Important safety instructions and additional information
- Important information regarding safety
- Disposal of the system
- Product safety
- General care
- Accessory box
- Meter
- Power off meter
- Automatic power-off
- Shut down meter
- Automatic shutdown
- Battery Pack
- Touchscreen
- Electromagnetic compatibility (EMC)
- Electrostatic discharge (ESD)
- Wireless connectivity
- Radiofrequency radiation exposure information
- Local Area Network: protection from unauthorized access
- Wired network connection
- 1.3 System components
- 1.4 Overview of the meter
- 1.5 Overview of the code key reader
- 1.6 Overview of the Accu-Chek Inform II Base Unit
- 1.7 Overview of the Accu-Chek Inform II Base Unit Hub
- 1.8 Overview of the accessory box
- 1.9 Reagents and consumables
- 1.10 Instructions for initial setup
- 2 Powering Up and Entering an Operator ID
- 3 Patient Glucose Testing
- 3.1 Information regarding blood glucose testing
- 3.2 Performing a patient glucose test
- Overview of test procedure
- Entering or selecting the patient ID
- Entering the patient ID manually
- Selecting the patient ID from a list
- Entering a patient ID with barcode scanner
- Confirming or selecting the test strip lot
- Patient identification information
- Inserting test strips
- Obtaining a blood sample
- Applying a blood sample
- Results screen
- Adding comments
- Add barcode content to a result
- Additional Patient Test
- 4 Glucose Control Testing
- 5 Review Results
- 6 Storing Test Strip, Control Solution, and Linearity Solution Information in the Meter
- 7 Linearity Testing
- 8 Proficiency Testing
- 9 Initial Startup
- 9.1 Connecting the base unit
- 9.2 Installing or replacing the battery pack
- 9.3 Docking the meter
- 9.4 Initial setup on the meter
- 9.5 Opening the Setup Menu
- 9.6 Date and time format
- 9.7 Display options and optional tests
- 9.8 Options for test strips
- 9.9 Options for glucose control tests
- 9.10 Value ranges (normal, critical, reportable)
- 9.11 Options for Operator ID Entry
- 9.12 Patient ID options
- 9.13 Creating a setup password
- 9.14 Setting the date and time
- 9.15 Beeper options
- 10 Maintenance and Care
- 11 Troubleshooting
- 12 General Product Information
- A Appendix
- B Appendix
- C Supplement for Other Test Entry
- D Supplement for Observed Test Sequence
- E Supplement for Enhanced Workflows
- F Appendix for Accu-Chek Inform II Base Unit (legacy version)
- G Limited Warranty
- Index
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08424705001 (04) 2021-06 USA • Accu-Chek Inform II Operator’s Manual Version 7.2
Disposal of the system
Product safety Observe the following information to ensure product
safety:
■ The system is suitable for continuous operation.
■ The system is not protected against the harmful
ingress of fluids (IP X0 rating according to
IEC 60529).
WARNING
Avoidance of electrical shock, fire, and explosions
■ Only use Roche original accessories (cables, power
supply units, battery packs, and spare parts). Third-
party cables, power supply units, and battery packs
can cause the battery pack to explode or the meter to
become damaged.
■ Do not use loose power sockets or damaged power
supply units, cables, plugs, or battery packs.
■ Do not short circuit the power supply unit, the base
unit charging contacts, or the battery pack.
■ Do not drop the Accu-Chek Inform II meter, the power
supply unit, or the battery pack and protect these
against shaking and vibrations.
WARNING
Infection by a potentially biohazardous instrument
The Accu-Chek Inform II system or its components must
be treated as potentially biohazardous waste. Decontam-
ination (i.e., a combination of processes including clean-
ing, disinfection and/or sterilization) is required before
reuse, recycling, or disposal.
Dispose of the system or its components according to the
appropriate local regulations or your facility policy. For
more information, contact Roche Customer Support
Center.