EN ISO 10993-15:2009

Name: EN ISO 10993-15:2009
Brand: CEN
SKU: EN ISO 10993-15:2009
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Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) EN ISO 10993-15:2009

Publication date: Aug 20, 2010

General information

Current stage: 99.60 Withdrawal effective May 24, 2023

Originator: CEN

Owner: CEN/TC 206 Biological and clinical evaluation of medical devices

Type: European Norm

ICS: 11.100.20 Biological evaluation of medical devices

Buying

Status: Withdrawn

Related legislation

Legislation related to this standard

98/79/EC

In vitro diagnostic medical devices

Legislation 98/79/EC

93/42/EEC

Medical devices

Harmonized/Supporting

Legislation 93/42/EEC

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

Legislation 2007/47/EC

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 10993-15:2000

NOW

WITHDRAWN
EN ISO 10993-15:2009
99.60 Withdrawal effective
May 24, 2023

REVISED BY

PUBLISHED
EN ISO 10993-15:2023