2. Getting involved
3. Standards Committees
4. DKE

DKE German Commission for Electrical, Electronic & Information Technologies of DIN and VDE

Abstract

This part of the international IEC 60601 standard-series supplements the general standard IEC 60601-1:2005+AMD:2012 with essential safety and performance requirements for appliances intended to induce photobiological effects in humans for therapeutic, diagnostic, monitoring or cosmetic/aesthetic purposes and equipped for this purpose with one or more optical (non-laser) radiation sources of risk group 1C (provided the embedded optical radiation source is of risk group 3) or 3 whose emission is in the wavelength range from 200 nm to 3 000 nm.

Begin

2022-02-10

Planned document number

DIN EN IEC 60601-2-57

Project number

02230773

Responsible national committee

DKE/K 812 - Elektromedizinische Geräte  

draft standard

Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use (IEC 76/696/CD:2021); Text in German and English
2023-03
Order from DIN Media

previous edition(s)

Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use (IEC 60601-2-57:2011); German version EN 60601-2-57:2011
2011-11