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ISO 18113-3:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use ISO 18113-3:2009

Publication date:   Dec 9, 2009

95.99 Withdrawal of Standard   Oct 6, 2022

General information

95.99 Withdrawal of Standard   Oct 6, 2022

ISO

ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems

International Standard

11.100.10   In vitro diagnostic test systems

Buying

Withdrawn

Language in which you want to receive the document.

Scope

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.
ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
ISO 18113-3:2009 can also be applied to accessories, where appropriate.

Life cycle

NOW

WITHDRAWN
ISO 18113-3:2009
95.99 Withdrawal of Standard
Oct 6, 2022

REVISED BY

PUBLISHED
ISO 18113-3:2022