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E DIN EN IEC 61326-2-6 VDE 0843-20-2-6:2025-07

Electrical equipment for measurement, control and laboratory use – EMC requirements

Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment

(IEC 65A/1174/FDIS:2025); German and English version FprEN IEC 61326-2-6:2025
Class/Status: Draft, valid
Released: 2025 -07 Published: 2025-06 -27
VDE Art. No.: 1800817
End of objection deadline: 2025-08-27

Note: You can pre-order this document (delivery subject to availability). Valid from 2025-07-01.

In addition to the scope of IEC 61326-1, this part of IEC 61326 series specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.

This Document is related to the following Topics (in bold):

11	HEALTH CARE TECHNOLOGY
11.020	Medical sciences and health care facilities in general
11.040	Medical equipment
11.060	Dentistry
11.080	Sterilization and disinfection
11.100	Laboratory medicine
11.140	Hospital equipment
11.180	Aids for disabled or handicapped persons
33	TELECOMMUNICATIONS. AUDIO AND VIDEO ENGINEERING
33.020	Telecommunications in general
33.040	Telecommunication systems
33.050	Telecommunication terminal equipment
33.060	Radiocommunications
33.070	Mobile services
33.100	Electromagnetic compatibility (EMC)
33.120	Components and accessories for telecommunications equipment
33.140	Special measuring equipment for use in telecommunications
33.160	Audio, video and audiovisual engineering
33.170	Television and radio broadcasting
33.180	Fibre optic communications
33.200	Telecontrol. Telemetering

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E DIN EN IEC 61326-2-6 VDE 0843-20-2-6:2025-07

Electrical equipment for measurement, control and laboratory use – EMC requirements

Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment

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