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SRPS EN ISO 16672:2012

Ophthalmic implants - Ocular endotamponades (ISO 16672:2003)

Jan 30, 2012
95.99   Withdrawal of Standard   Aug 30, 2016

General information

95.99     Aug 30, 2016

ISS

Z172

European Norm

11.040.70  

English  

From plan 2011

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Scope

ISO 16672:2003 applies to ocular endotamponades (OEs), a group of non-solid implants used in ophthalmology to flatten and position a detached retina onto the choroid, or to tamponade the retina.
With regard to the safety and efficacy of OEs, ISO 16672:2003 specifies requirements for their intended performance, design attributes, pre-clinical and clinical evaluation, sterilization, product packaging, product labelling and the information supplied by the manufacturer.

Life cycle

NOW

WITHDRAWN
SRPS EN ISO 16672:2012
95.99 Withdrawal of Standard
Aug 30, 2016

REVISED BY

WITHDRAWN
SRPS EN ISO 16672:2016

Related project

Adopted from EN ISO 16672:2003

Adopted from ISO 16672:2003 IDENTICAL