STANDARD

Current

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 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.

General information on ÖNORM EN ISO 15197

Format
Paper | 61 Pages
Language
German | English | Download GER/ENG
Publisher
Austrian Standards International

Timeline

An overview of the development of ÖNORM EN ISO 15197 from 2003 til today.

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Normative References

Here you will find an extract of the normative references. Please refer to the document itself for the full list.

Dokumentnummer Titel Ausgabedatum Art Link
Dokumentnummer
ISO 13485:2016
Titel
Medical devices — Quality management systems — Requirements for regulatory purposes
Ausgabedatum
2016 02 25
Art
Standard
Dokumentnummer
ISO 14971:2019
Titel
Medical devices — Application of risk management to medical devices
Ausgabedatum
2019 12 10
Art
Standard
Dokumentnummer
ISO 17511:2020
Titel
In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Ausgabedatum
2020 04 24
Art
Standard
Dokumentnummer
ISO 18113-1:2009
Titel
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Ausgabedatum
2009 12 09
Art
Standard
Dokumentnummer
ISO 18113-4:2009
Titel
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
Ausgabedatum
2009 12 17
Art
Standard
Dokumentnummer
ISO 18113-5:2009
Titel
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
Ausgabedatum
2009 12 09
Art
Standard
Dokumentnummer
ISO 23640:2011
Titel
In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
Ausgabedatum
2011 11 29
Art
Standard

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