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EVS-EN ISO 10993-1:2011

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)

Üldinfo
Kehtiv alates 03.02.2011
Alusdokumendid
ISO 10993-1:2009; EN ISO 10993-1:2009
Standardi ajalugu
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Põhitekst
prEN ISO 10993-1
03.02.2011
Põhitekst
06.09.2010
Parandus
This part of ISO 10993 describes: - the general principles governing the biological evaluation of medical devices within a risk management process; - the general categorization of devices based on the nature and duration of their contact with the body; - the evaluation of existing relevant data from all sources; - the identification of gaps in the available data set on the basis of a risk analysis; - the identification of additional data sets necessary to analyse the biological safety of the medical device; - the assessment of the biological safety of the medical device. This part of ISO 10993 does not cover testing of materials and devices that do not come into direct or indirect contact with the patient's body, nor does it cover biological hazards arising from any mechanical failure. Other parts of ISO 10993 cover specific tests, as indicated in the Foreword.
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EVS-EN ISO 15223-1:2016

Meditsiiniseadmed. Meditsiiniseadme märgisel, märgistusel ning kaasuvas teabes kasutatavad tingmärgid. Osa 1: Üldnõuded
Uusim versioon Kehtiv alates 03.01.2017
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EVS-EN ISO 10993-10:2013

Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
Uusim versioon Kehtiv alates 07.10.2013
Põhitekst + parandus

EVS-EN ISO 13485:2016

Meditsiiniseadmed. Kvaliteedijuhtimissüsteemid. Normatiivsed nõuded
Uusim versioon Kehtiv alates 02.03.2016
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EVS-EN 1041:2008+A1:2013

Tootja antav info meditsiiniseadmete kohta
Uusim versioon Kehtiv alates 14.11.2013