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UNE-EN ISO 18113-2:2025

Current

Current

The latest, up-to-date edition.

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

Available format(s)

Hardcopy , PDF

Language(s)

Spanish, Castilian, English

Published date

22-01-2025

€88.80
Excluding VAT

This document specifies requirements for information supplied by the manufacturer of IVD reagents,calibrators and controls intended for professional use.This document can also be applied to accessories.This document applies to the labels for outer and immediate containers and to the instructions for use.This document does not apply to:a) IVD instruments or equipment;b) IVD reagents for self-testing.

Committee
CTN 129
DocumentType
Standard
Pages
28
PublisherName
Asociación Española de Normalización
Status
Current

Standards Relationship
ISO 18113-2:2022 Identical
EN ISO 18113-2:2024 Identical

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€88.80
Excluding VAT