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NEN-EN-ISO 10993-1:2009-10

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process

Available format(s)

Hardcopy

Language(s)

English

Published date

01-10-2009

Superseded date

25-10-2025

Superseded by

NEN-EN-ISO 10993-1:2020

€190.80
Excluding VAT

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.

Committee
TC 194
DocumentType
Standard
Pages
21
PublisherName
Netherlands Standards
Status
Superseded
SupersededBy

Standards Relationship
EN ISO 10993-1:2009 Identical
ISO 10993-1:2009 Identical

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€190.80
Excluding VAT