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SSH EN ISO 10993-9:2000

Vlerësimi biologjik i pajisjeve mjekësore - Pjesa 9: Kuadri për identifikimin dhe përcaktimin e anës sasiore të produkteve potenciale të shgraduara

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)
1 jan 2000
95.99 Withdrawal of Standard   30 dhj 2009

General information

95.99     30 dhj 2009

DPS

DPS/KT 316

European Norm

11.100  

anglisht  

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Scope

This part of ISO 10993 provides general principles for the systematic evaluation of the potential and observed biodegradation of medical devices and for the design and performance of biodegradation studies. This part of ISO 10993 is not applicable to: a) viable-tissue engineered products; b) methodologies for the generation of degradation products by mechanical processes. Methodologies for the production of this type of degradation product are described in specific product standards, where available; c) leachable components wich are not degradation products. Where product standards provide applicable product-specific methodologies for the identification and quantification of degradation products, those standards shall be considered as alternatives.

Related directives

Directives related to this standards.

90/385/EEC

Pajisjet mjekësore aktive transplatuese

Të harmonizuara
93/42/EEC

Pajisje Mjekësore

Të harmonizuara

Life cycle

PREVIOUSLY

PUBLISHED
SSH EN ISO 10993-9:2009

NOW

WITHDRAWN
SSH EN ISO 10993-9:2000
95.99 Withdrawal of Standard
30 dhj 2009

Related project

Adopted from EN ISO 10993-9:1999