IEC 61010-2-101 Measurement - Control and Laboratory Use - Safety Requirements for Electrical Equipment - Special Requirements for In Vitro Diagnostic (IVD) Medical Equipment

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IEC 61010-2-101 Measurement - Control and Laboratory Use - Safety Requirements for Electrical Equipment - Special Requirements for In Vitro Diagnostic (IVD) Medical Equipment

IEC 61010-2-101 is also available as IEC 61010-2-101 RLV which includes the international standard and redline version and shows all the changes in technical content compared to the previous version.

IEC 61010-2-101 Measurement - Control and Laboratory Use - Safety Requirements for Electrical Equipment - Special Requirements for In Vitro Diagnostic (IVD) Medical Equipment

IEC 61010-2-101 applies to equipment for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication as specified in IEC Guide 104. This standard has been prepared in close collaboration with the CENELEC BTTF 88.1 working group.

This edition includes the following important technical changes from the previous edition:

  • Adaptation of the changes introduced by the 61010st Amendment of IEC 1-1;
  • Added tolerance for stability of AC voltage test equipment.

EUROLAB assists manufacturers with IEC 61010-2-101 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.

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