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SRPS EN ISO 10993-14:2011

Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)

Jun 28, 2011
Jun 28, 2011

General information

60.60     Jun 28, 2011

ISS

Z076

European Norm

11.100.20  

Serbian  

From plan 2011

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Published

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Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized
Directive 93/42/EEC
98/79/EC

In vitro diagnostic medical devices

Directive 98/79/EC
2007/47/EC

Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

Directive 2007/47/EC

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN ISO 10993-14:2008

NOW

PUBLISHED
SRPS EN ISO 10993-14:2011
60.60 Standard published
Jun 28, 2011

REVISED BY

PROJECT
prSRPS EN ISO 10993-14:2024

Related project

Adopted from EN ISO 10993-14:2009

Adopted from ISO 10993-14:2001 IDENTICAL