In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022, IDT)

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Hardcopy

Language(s)

English

Published date

02-09-2024

Publisher

Standardiserings-Kommissionen I Sverige

€281.25

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This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

Committee	ISO/TC 212
DocumentType	Standard
Pages	68
PublisherName	Standardiserings-Kommissionen I Sverige
Status	Current
Supersedes	SS-EN ISO 18113-1 : 2011

Standards	Relationship
ISO 18113-1:2022	Identical
EN ISO 18113-1:2024	Identical

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SS-EN ISO 18113-1:2024

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022, IDT)

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SS-EN ISO 18113-1:2024

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022, IDT)

Abstract

General Product Information

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