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IEC 60601-2-75 Consolidated version

IEC 60601-2-75:2017+AMD1:2023 CSV
Medical electrical equipment - Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment
IEC 60601-2-75:2017+AMD1:2023 CSV applies to the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment. Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of the general standard. This document applies to photodynamic therapy and photodynamic diagnosis equipment used for compensation or alleviation of disease, injury or disability. In the case of combined equipment (e.g. equipment additionally provided with a function or an applied part for the target area), such equipment also comply with any particular standard specifying safety requirements for the additional function. This particular standard does not apply to:
- light therapy equipment intended for use in photothermal ablation, coagulation, and hyperthermia;
- low-level laser therapy equipment not intended for use with a photosensitizer;
- illumination equipment intended for use in observation, monitoring, and diagnosis, not intended for use with a photosensitizer.
This document is to be used with IEC 60601-1:2005 and its amendment 1.
CONSOLIDATED VERSION
English/French

Technical committee

TC 62/SC 62D Particular medical equipment, software, and systems

Category

Safety
Publication typeInternational Standard
Publication date2023-01-30
Edition1.1
ICS

11.040.01

Stability date2030
ISBN number9782832264386
Pages131
File size1.60 MB
EditionDatePublicationEditionStatus
  • Ensure healthy lives and promote well-being for all

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