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Norm

ÖNORM EN ISO 15197

Issue date: 2015 12 15

In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)

This International Standard specifies requirements for in vitro glucose monitoring systems that measure glucose concentrations in capillary blood samples, for specific de...
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Valid
Publisher:
Austrian Standards International
Format:
Digital | 61 Pages
Language:
German | English
Optionally co-design standards:
This International Standard specifies requirements for in vitro glucose monitoring systems that measure glucose concentrations in capillary blood samples, for specific design verification procedures and for the validation of performance by the intended users. These systems are intended for self-measurement by lay persons for management of diabetes mellitus. This International Standard is applicable to manufacturers of such systems and those other organizations (e.g. regulatory authorities and conformity assessment bodies) having the responsibility for assessing the performance of these systems. This International Standard does not: - provide a comprehensive evaluation of all possible factors that could affect the performance of these systems, - pertain to glucose concentration measurement for the purpose of diagnosing diabetes mellitus, - address the medical aspects of diabetes mellitus management, - apply to measurement procedures with measured values on an ordinal scale (e.g. visual, semiquantitative measurement procedures), or to continuous glucose monitoring systems, - apply to glucose meters intended for use in medical applications other than self-testing or the management of diabetes mellitus.
ÖNORM EN ISO 15197
2015 12 15
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testin...
Norm
ÖNORM EN ISO 15197
2013 12 15
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testin...
Norm
ÖNORM EN ISO 15197
2013 09 01
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testin...
Norm
ÖNORM EN ISO 15197
2005 05 01
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testin...
Norm
ÖNORM EN ISO 15197
2003 10 01
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testin...
Norm
Historie aufklappen
Final Draft
ISO/FDIS 13485
Issue date : 2015 10 29
Medical devices — Quality management systems — Requirements for regulatory purposes
Norm
ISO 13485:2003
Issue date : 2003 07 03
Medical devices — Quality management systems — Requirements for regulatory purposes
Norm
ISO 14971:2007
Issue date : 2007 02 28
Medical devices — Application of risk management to medical devices (Corrected version 2007-09)
Norm
ISO 17511:2003
Issue date : 2003 08 22
In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materials
Norm
ISO 18113-1:2009
Issue date : 2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Norm
ISO 18113-4:2009
Issue date : 2009 12 17
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
Norm
ISO 18113-5:2009
Issue date : 2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
Norm
ISO 23640:2011
Issue date : 2011 11 29
In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
Norm
ÖNORM EN 13612
Issue date : 2002 08 01
Performance evaluation of in vitro diagnostic medical devices
Norm
ISO 13485:2016
Issue date : 2016 02 25
Medical devices — Quality management systems — Requirements for regulatory purposes
Norm
ISO 14971:2019
Issue date : 2019 12 10
Medical devices — Application of risk management to medical devices
Norm
ISO 17511:2020
Issue date : 2020 04 24
In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Norm
ISO 18113-1:2009
Issue date : 2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Norm
ISO 18113-4:2009
Issue date : 2009 12 17
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
Norm
ISO 18113-5:2009
Issue date : 2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
Norm
ISO 23640:2011
Issue date : 2011 11 29
In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
Norm
ISO 15197:2013
Issue date : 2013 05 14
In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus