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Service and disposal
The Analyzer should be cleaned as recommended under section Maintenance prior
to service or disposal. Dispose of the battery lid and cuvette holder as potentially
infectious waste. Remove the batteries. Clean the Analyzer cover and optical parts
according to section Maintenance. Disinfect the Analyzer external surfaces and opti-
cal parts according to local procedures. Wait for three weeks, then dispose of the
Analyzer according to local procedures for electronic waste. For further information,
contact HemoCue distributor or HemoCue AB.
EMC and Electrical Safety
The analyzer has been tested and complies with following standards:
• IEC/EN 61010-1
• IEC/EN 61010-2-101
• IEC/EN 61326-2-6 (including applicable parts of IEC/EN 61326-1)
The analyzer has been tested for indoor use. It is recommended to evaluate the elec-
tromagnetic environment prior to use of the device.
Do not use this device in close proximity to sources of strong electromagnetic radia-
tion (e.g unshielded intentional RF sources), as these can interfere with the proper
operation.
Note: It is the manufacturer's responsibility to provide equipment electromagnetic
compatibility information to the customer or user.
Note: It is the user's responsibility to ensure that a compatible electromagnetic envi-
ronment for the equipment can be maintained in order that the device will perform
as intended.
Spare parts
Optional items
• Power adapter*
• Printer
• Battery Lid
• Software applications
• Cuvette holder
• Cables for PC and printer connection
• HemoCue Cleaners
• Hard Carrying Case
• HemoCue Safety Lancets
* Not available in all countries
References
• NIST Standard reference material, https://www.nist.gov/srm.
• Atkin et al, Annals of Internal Medicine, 1991, 114;12, 1020–1024.
• Hannestad et al, Accuracy and precise isotope dilution mass spectrometry
method for determining glucose in whole blood, Clinical Chemistry, 1997;
43:5, 794–800.
• Rifai, Tietz Fundamentals of Clinical Chemistry and Molecular Diagnostics,
8th Ed., Elsevier, 2018.
• Definition and Diagnosis of Diabetes Mellitus and Intermediate
Hyperglycaemia. Report of a WHO/IDF Consultation. Geneva: WHO 2006.
• Definition, Diagnosis and Classification of Diabetes Mellitus and its
Complications. Report of a WHO Consultation. Geneva: WHO 1999.
• American Diabetes Association. Diagnosis and Classification of Diabetes
Mellitus, Diabetes Care, 2006, 29: S43–S48.
• Interference Testing in Clinical Chemistry NCCLS Approved Guideline; CLSI
Document EP7-A2 Vol. 25 No. 27.
• HemoCue Glucose 201 RT Microcuvettes Package Insert.
Reporting of serious incidents
If, during the use of this device or as a result of its use, a serious incident has
occurred, please report it to HemoCue AB or local distributor, and to your
national authority as applicable according to local requirements.
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