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
Patient Glucose Testing • 3
63
08424705001 (04) 2021-06 USA • Accu-Chek Inform II Operator’s Manual Version 7.2
■ The System Measuring Range refers to the meas-
urement range of the system itself (strips and
meter) and is the only range which cannot be con-
figured. With Accu-Chek Inform II test strips this
fixed range is 10 to 600 mg/dL (0.6 to 33.3 mmol/L).
If a result falls outside this range, the message HI or
LO appears, i.e., the result cannot be quantified.
■ Glucose results above or below the Reportable
Range, as defined by the institution or local regula-
tory body, are above the highest or below the
lowest numerical results to be reported. Results
outside this range must not be used for intervention
decisions.
■ Glucose results above or below the Critical Range,
as defined by the institution, require immediate
action as defined by hospital policy.
■ Glucose results within the Normal Range, as
defined by the institution, are considered normal
and require no therapeutic action.
Patient Test
Out of Reportable Range
RR HI
Patient 123456789
12:48 pm
03/17/20
Date 03/17/20 12:48 pm
Patient Test
Out of Normal Range
220
Patient 123456789
Date 03/17/20 12:48 pm
mg/dL
12:48 pm
03/17/20
Patient Test
Out of Critical Range
305
Patient 123456789
Date 03/17/20 12:48 pm
mg/dL
12:48 pm
03/17/20
Patient Test
Out of Crit. Range
34
Patient 123456789
Date 03/17/20 12:48 pm
mg/dL
12:48 pm
03/17/20
Patient Test
Out of Critical Range
CR LO
Patient 123456789
Date 03/17/20 12:48 pm
12:48 pm
03/17/20