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ISO 18113-3:2022

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
6 tet 2022

General information

60.60     6 tet 2022

ISO

ISO/TC 212

International Standard

11.100.10  

anglisht   frëngjisht  

Buying

Publikuar

Language in which you want to receive the document.

Scope

This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use.
This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
This document can also be applicable to accessories.
This document does not apply to:
a) instructions for instrument servicing or repair;
b) IVD reagents, including calibrators and control materials for use in control of the reagent;
c) IVD instruments for self-testing.

Life cycle

PREVIOUSLY

WITHDRAWN
ISO 18113-3:2009

NOW

PUBLISHED
ISO 18113-3:2022
60.60 Standard published
6 tet 2022

National adoptions

SSH ISO 18113-3:2022  
DPS

Pajisje mjekësore për diagnostikimin in vitro - Informacioni i dorëzuar nga prodhuesi (etiketimi) - Pjesa 3: Instrumentet e diagnostikimit in vitro për përdorim profesional

60.60 Standard published

DPS/KT 140 më tepër