Publikuar
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.
WITHDRAWN
ISO 18113-3:2009
PUBLISHED
ISO 18113-3:2022
60.60
Standard published
6 tet 2022
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
Pajisje mjekësore diagnostike in vitro - Informacioni i dhënë nga prodhuesi (etiketimi) - Pjesa 3: Instrumente diagnostikues in vitro për profesionistë (ISO 18113-3:2022)
60.60 Standard published
English