EN ISO 10993-6:2007

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) EN ISO 10993-6:2007

Publication date:   Dec 20, 2008

General information

99.60 Withdrawal effective   May 20, 2009

CEN

CEN/TC 206 Biological and clinical evaluation of medical devices

European Norm

11.100.20   Biological evaluation of medical devices

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Scope

This part of ISO 10993 specifies test methods for the assessment of the local effects of an implant material on living tissue, at both the macroscopic and microscopic level. The test specimen is implanted into a site and tissue appropriate for evaluation of the biological safety of the material. The implant is not intended to be subjected to mechanical or functional loading. The local effects are evaluated by a comparison of the tissue response caused by a test specimen to that caused by materials used in medical devices whose clinical acceptability has been established. The test methods for local effects after implantation are used to assess subchronic effects (short-term, up to 12 weeks), or chronic effects (long-term, longer than 12 weeks).

Related legislation

Legislation related to this standard

90/385/EEC

Active implantable medical devices

Harmonized/Supporting
93/42/EEC

Medical devices

Harmonized/Supporting

Life cycle

PREVIOUSLY

WITHDRAWN
EN 30993-6:1994

NOW

WITHDRAWN
EN ISO 10993-6:2007
99.60 Withdrawal effective
May 20, 2009

REVISED BY

WITHDRAWN
EN ISO 10993-6:2009