Cover E DIN EN IEC 60601-2-57 VDE 0750-2-57:2023-03
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E DIN EN IEC 60601-2-57 VDE 0750-2-57:2023-03

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
Class/Status: Draft, valid
Released: 2023 -03   Published: 2023-02 -24
VDE Art. No.: 1701787
End of objection deadline: 2023-04-24

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.

Title Format
Entwicklung und Herstellung medizinischer Software
Prinz, Thorsten (Hrsg.)

Entwicklung und Herstellung medizinischer Software

Normen in der Medizintechnik
VDE-Schriftenreihe – Normen verständlich, Band 171

2017, 219 pages, Din A5, Broschur

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