EN ISO 10993-16:2009

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) EN ISO 10993-16:2009

General information

Current stage: 99.60 Withdrawal effective Feb 15, 2010

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

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Harmonized/Supporting

90/385/EEC

Active implantable medical devices

Harmonized/Supporting

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

PREVIOUSLY

WITHDRAWN
EN ISO 10993-16:1997

NOW

WITHDRAWN
EN ISO 10993-16:2009
99.60 Withdrawal effective
Feb 15, 2010

REVISED BY

WITHDRAWN
EN ISO 10993-16:2010

EN ISO 10993-16:2009

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) EN ISO 10993-16:2009

General information

Related legislation

93/42/EEC

90/385/EEC

2007/47/EC

Life cycle

PREVIOUSLY

NOW

REVISED BY

Relations

Adopted from ISO 10993-16:1997 IDENTICAL