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SSH EN ISO 10993-12:2012

Vlerësimi biologjik i pajisjeve mjekësore - Pjesa 12: Përgatitja e mostrës dhe e materialeve referuese (ISO 10993-12:2012)

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)
26 pri 2013

General information

60.60     26 pri 2013

DPS

DPS/KT 316

European Norm

11.100.20  

anglisht  

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Scope

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.

Related directives

Directives related to this standards.

93/42/EEC

Pajisje Mjekësore

Të harmonizuara
90/385/EEC

Pajisjet mjekësore aktive transplatuese

Të harmonizuara
2007/47/EC

Direktiva 2007/47/EC e Parlamentit Europian dhe e Këshillit të 5 shtator 2007 amendon Direktivën e Këshillit 90/385/EEC mbi përafrimin e ligjeve të Shteteve Anëtare në lidhje me pajisje medicinale aktive transplatuese, Direktiva e Këshillit 93/42/EEC në lidhje me pajisjet mjekësore dhe Direktivën 98/8/EC në lidhje me vendosjen e produkteve biocide në treg

Të harmonizuara

Life cycle

PREVIOUSLY

Replaces
SSH EN ISO 10993-12:2009

NOW

PUBLISHED
SSH EN ISO 10993-12:2012
60.60 Standard published
26 pri 2013

Related project

Adopted from EN ISO 10993-12:2012

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