EN ISO 18113-1:2011

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

Publication date:   Feb 17, 2012

General information

99.60 Withdrawal effective   Jun 12, 2024

CEN

CEN/TC 140 In vitro diagnostic medical devices

European Norm

11.100.10   In vitro diagnostic test systems

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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.

Related legislation

Legislation related to this standard

98/79/EC

In vitro diagnostic medical devices

Harmonized/Supporting

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 18113-1:2009

NOW

WITHDRAWN
EN ISO 18113-1:2011
99.60 Withdrawal effective
Jun 12, 2024

REVISED BY

PUBLISHED
EN ISO 18113-1:2024

Relations

Adopted from ISO 18113-1:2009 IDENTICAL