BAS EN ISO 10993-12:2013
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
General Information
Status: Withdrawn
No. of pages: 25
Language: English
Edition: 5.
Adoption method: Endorsment
Publication date: 21.11.2013
Technical committee:
Directive:
90/385/EEC, Active implantable medical devices
93/42/EEC, Medical devices;
93/42/EEC, Medical devices;
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Abstract
ISO 10993-12:2012 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of ISO 10993. Specifically, ISO 10993-12:2012 addresses the following:
test sample selection;
selection of representative portions from a device;
test sample preparation;
experimental controls;
selection of, and requirements for, reference materials;
preparation of extracts.
ISO 10993-12:2012 is not applicable to live cells, but can be relevant to the material or device components of combination products containing live cells.
Lifecycle
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Original document and degree of correspondence
- EN ISO 10993-12:2012, identical
- ISO 10993-12:2012, identical