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IEC 60601-2-57 Ed. 2.0 b:2023

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, cosmetic and aesthetic use
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IEC 60601-2-57 Ed. 2.0 b:2023

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, cosmetic and aesthetic use

PUBLISH DATE 2023
PAGES 64
IEC 60601-2-57 Ed. 2.0 b:2023
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, cosmetic and aesthetic use
IEC 60601-2-57:2023 applies to basic safety and essential performance of equipment incorporating one or more sources of optical radiation in the wavelength range 200 nm to 3 000 nm, with the exception of laser radiation, and intended to create photobiological effects in humans for therapeutic, diagnostic, monitoring, and cosmetic or aesthetic applications; hereafter referred to as light source equipment (ls equipment).
SDO IEC: International Electrotechnical Commission
Document Number IEC 60601
Publication Date July 1, 2023
Language b - English & French
Page Count 64
Revision Level 2.0
Supercedes
Committee 76
Publish Date Document Id Type View
July 1, 2023 Revision
July 1, 2023 IEC 60601-2-57 Ed. 2.0 b:2023 Revision