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EN ISO 18113-4:2009

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) EN ISO 18113-4:2009

Publication date:   Mar 22, 2010

General information

99.60 Withdrawal effective   Oct 19, 2011

CEN

CEN/TC 140 In vitro diagnostic medical devices

European Norm

11.100.10   In vitro diagnostic test systems

Buying

Withdrawn

Language in which you want to receive the document.

Scope

ISO 18113-4:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for self-testing.
ISO 18113-4:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for self-testing.
ISO 18113-4:2009 can also be applied to accessories, where appropriate.
ISO 18113-4:2009 applies to the labels for outer and immediate containers and to the instructions for use.

Related legislation

Legislation related to this standard

98/79/EC

In vitro diagnostic medical devices

Harmonized/Supporting
Legislation 98/79/EC

Life cycle

PREVIOUSLY

WITHDRAWN
EN 376:2002

NOW

WITHDRAWN
EN ISO 18113-4:2009
99.60 Withdrawal effective
Oct 19, 2011

REVISED BY

WITHDRAWN
EN ISO 18113-4:2011