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ISO 18113-2:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
9 dhj 2009
95.99 Withdrawal of Standard   6 tet 2022

General information

95.99     6 tet 2022

ISO

ISO/TC 212

International Standard

11.100.10  

anglisht   frëngjisht  

Buying

Shfuqizuar

Language in which you want to receive the document.

Scope

ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
ISO 18113-2:2009 can also be applied to accessories.
ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.

Life cycle

NOW

WITHDRAWN
ISO 18113-2:2009
95.99 Withdrawal of Standard
6 tet 2022

REVISED BY

PUBLISHED
ISO 18113-2:2022