Biological evaluation of medical devices -- Part 6: Tests for local effects after implantation
This standard has been revised by: ISO 10993-6:2016
ISO 10993-6:2007 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices.
ISO 10993-6:2007 applies to materials that are:
- solid and non-biodegradable;
- degradable and/or resorbable;
- non-solid, such as porous materials, liquids, pastes and particulates.
ISO 10993-6:2007 may also be applied to medical devices that are intended to be used topically in clinical indications where the surface or lining may have been breached, in order to evaluate local tissue responses.
This part of ISO 10993 does not deal with systemic toxicity, carcinogenicity, teratogenicity or mutagenicity. However, the long-term implantation studies intended for evaluation of local biological effects may provide insight into some of these properties. Systemic toxicity studies conducted by implantation may satisfy the requirements of ISO 10993-6:2007.
Document published on: 2007-04-15 Edition: 2 (Monolingual) ICS: 11.100.20 Status: Withdrawn Stage: 95.99 (2016-11-28) TC/SC: ISO/TC 194 Number of Pages:
Revised by: ISO 10993-6:2016
Revises: ISO 10993-6:1994
No corrigenda or amendments available