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EN IEC 60601-2-83:2020 Standard

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  Keywords:

#equipment #amendment #requirements #light #home

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment

  Purpose

Amendment to EN IEC 60601-2-83:2020

  Publication

Wednesday 14th of April 2021

  Related Standards

EN 14931:2006

Medical devices Directive (93/42/EEC)

Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety re...

EN ISO 15883-4:2018

Medical devices Directive (93/42/EEC)

Washer-disinfectors - Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endo...

EN ISO 14155:2020

Medical devices Directive (93/42/EEC)

Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

EN ISO 11607-2:2020

Medical devices Directive (93/42/EEC)

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes ...

EN ISO 11607-1:2020

Medical devices Directive (93/42/EEC)

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging sy...

EN 1789:2020

Medical devices Directive (93/42/EEC)

Medical vehicles and their equipment - Road ambulances

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