EN IEC 61010-2-101:2022/prAB
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101 Particular requirements for in vitro diagnostic (IVD) medical equipment

Standard No.
EN IEC 61010-2-101:2022/prAB
Release Date
1970
Published By
European Committee for Electrotechnical Standardization（CENELEC）
Status
Replace By
EN IEC 61010-2-101:2022/A11:2022
Latest
EN IEC 61010-2-101:2022/A11:2022
Scope
The scope of the Amendment A12 is the same as EN 61010-2-101:2022. It applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. A12 shall include Annex zz to achieve harmonization under the IVD Regulation 746/2017/EU

EN IEC 61010-2-101:2022/prAB history

  • 2022 EN IEC 61010-2-101:2022/A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
  • 2022 EN IEC 61010-2-101:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment


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