DIN EN ISO 18113-1:2021-09

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2021); German and English version prEN ISO 18113-1:2021

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Publisher	Deutsche Institut für Normung e.V. (DIN)
Publication Date	09/01/2021
Page Count	8
EAN	---
ISBN	---
Weight (in grams)	---

Replaces

DIN EN ISO 18113-1:2013-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011.

01/01/2013

Superseded

Historical

Previous versions

DIN EN ISO 18113-1:2024-10

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022); German version EN ISO 18113-1:2024

01/10/2024

Active

Most Recent

DIN EN ISO 18113-1:2021-09

01/09/2021

Superseded

Historical

DIN EN ISO 18113-1:2013-01

01/01/2013

Superseded

Historical

DIN EN ISO 18113-1:2010-05

01/05/2010

Superseded

Historical

DIN EN ISO 18113-1:2007-02

Clinical laboratory testing and in vitro diagnostic medical systems - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2006); German version prEN ISO 18113-1:2006

01/02/2007

Superseded

Historical

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