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About This Item

 

Full Description

Scope and object: This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning one or more of the following:
  • a physiological or pathological state; or
  • a congenital abnormality;
  • the determination of safety and compatibility with potential recipients;
  • the monitoring of therapeutic measures.
Self-test IVD medical equipment is intended by the manufacturer for use by lay persons in a home environment.

NOTE If all or part of the equipment falls within the scope of one or more other Part 2 standards of the IEC 61010 series as well as within the scope of this document, consideration is given to those other Part 2 standards.
 

Document History

  1. CSA C22.2 NO. 61010-2-101:19

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    Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (Adopted IEC 61010-2-101:2018, third edition, 2018-10, with Canadian deviations)

    • Most Recent
  2. CAN/CSA C22.2 NO. 61010-2-101:15


    Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (Adopted IEC 61010-2-101:2015, second edition, 2015-01, with Canadian deviations)

    • Historical Version
  3. CAN/CSA C22.2 NO. 61010-2-101-04 (R2014)


    Safety Requirements for Electrical Equipment for Measurement, Control and Laboratory Use - Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment (Adopted CEI/IEC 61010-2-101:2002, first edition, 2002-01)

    • Historical Version