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ISO 18113-1:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements

Dec 9, 2009
95.99   Withdrawal of Standard   Oct 6, 2022

General information

95.99     Oct 6, 2022

ISO

ISO/TC 212

International Standard

11.100.10  

English   French  

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Scope

ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.

Life cycle

NOW

WITHDRAWN
ISO 18113-1:2009
95.99 Withdrawal of Standard
Oct 6, 2022

REVISED BY

PUBLISHED
ISO 18113-1:2022

National adoptions

SRPS EN ISO 18113-1:2011  
ISS

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

95.99   Withdrawal of Standard

Z076 more

SRPS EN ISO 18113-1:2013  
ISS

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

95.99   Withdrawal of Standard

Z076 more