prBAS EN IEC 61326-2-6:2026

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical electrical equipment


Opće informacije
Status:Projekt
Broj stranica:70
Metoda usvajanja:Proglašavanje
Jezik:engleski
Izdanje:2.
Nadnevak realizacije:17.11.2025
Predviđeni nadnevak naredne faze:27.11.2025
Tehnički komitet:BAS/TC 51, Automatika
Direktive:
2014/30/EU, Elektromagnetna kompatibilnost
ICS:
25.040.40, Mjerenje i upravljanje u industrijskim procesima
17.220.20, Mjerenje električnih i magnetskih veličina
33.100.20, Imunost

Apstrakt
IEC 61326-2-6:2025 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of IN VITRO DIAGNOSTIC MEDICAL ELECTRICAL EQUIPMENT (IVD MEE). This part of IEC 61326 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of IVD MEE in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted by IVD MEE. BASIC SAFETY with regard to electromagnetic disturbances is applicable to all IVD MEE. NOTE 1 Performance with respect to electromagnetic disturbances other than ESSENTIAL PERFORMANCE is the subject of IEC 61326-1:2020 NOTE 2 IT equipment can be a part of an IVD MEE, if it is required to maintain BASIC SAFETY or ESSENTIAL PERFORMANCE. This edition includes the following significant technical changes with respect to the previous edition: - Update of the document with respect to test levels and documentation.

Životni ciklus
...

Izvorni dokument i stepen usklađenosti
EN IEC 61326-2-6:2025, identičan
IEC 61326-2-6:2025, identičan

Veza sa BAS standardima

Radni materijal

Samo članovi tehničkog komiteta imaju pristup radnom materijalu. Ukoliko ste član, molimo prijavite se sa vašim nalogom i dobićete pristup dokumentima. Пријавите се