ISO 18113-1:2009

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

Publication date: 9 dhj 2009

95.99 Withdrawal of Standard 6 tet 2022

General information

Current stage: 95.99 Effective date: 6 tet 2022

Originator: ISO

Owner: ISO/TC 212

Type: International Standard

ICS: 11.100.10

Gjuha: anglisht frëngjisht

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Statusi: Shfuqizuar

PDF - 7 123 Lekë

Paper - 7 123 Lekë

CD - 7 123 Lekë

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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.

ISO 18113-1:2009

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

95.99 Withdrawal of Standard 6 tet 2022

General information

Buying

Scope

Life cycle

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