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SSH EN ISO 18113-4:2011

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

Mar 29, 2012

General information

60.60     Mar 29, 2012

DPS

DPS/KT 140

European Norm

11.100.10  

English  

Buying

Published

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 directives

Directives related to this standards.

98/79/EC

In vitro diagnostic medical devices

Harmonized

Life cycle

NOW

PUBLISHED
SSH EN ISO 18113-4:2011
60.60 Standard published
Mar 29, 2012

REVISED BY

IN_DEVELOPMENT
prSSH EN ISO 18113-4:2024

Related project

Adopted from EN ISO 18113-4:2011