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Homepage>UNE standards>UNE EN IEC 61010-2-101:2023 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
in stockReleased: 2023-09-27
UNE EN IEC 61010-2-101:2023 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment

UNE EN IEC 61010-2-101:2023

Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment

Requisitos de seguridad de equipos eléctricos de medida, control y uso en laboratorio. Parte 2-101: Requisitos particulares para equipos médicos para diagnóstico in vitro (DIV).

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Standard number:UNE EN IEC 61010-2-101:2023
Pages:24
Released:2023-09-27
Status:Standard
DESCRIPTION

This standard UNE EN IEC 61010-2-101:2023 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment is classified in these ICS categories:

  • 19.080
  • 11.040.55
Categories:
UNE standards
11.040.55 Diagnostic equipment
19.080 Electrical and electronic testing
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