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DS/ISO 10993-1:2018

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk management process (ISO/FDIS 10993-1:2018)

Published date

22-12-2020

Superseded date

07-01-2026

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This part document 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
DS/S-258
DocumentType
Standard
PublisherName
Danish Standards
Status
Superseded

Standards Relationship
ISO 10993-1:2018 Identical

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