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Registers collected 2026-08-22.See collection dates
ISO/IEC 17025 directory

IEC 60601-2-39 Accredited Testing Labs in United States

4 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-39 testing. From the accredited scope text: “IEC 60601-2-39 (Peritoneal Dialysis Equipment); EN/IEC 60601-2-40 (Electromyographs and Evoked Response Equipment); EN/IEC 60601-2-41 (Surgical Luminaires and Luminaires for Diagnosis); EN/IEC 60601-2” “IEC 60601-2-39; IEC 60601-2-39 Edition 3.0 2018-04; IEC 60601-2-44; IEC 60601-2-44 Edition 3.2 2016; IEC 60601-2-46; IEC 60601-2-47; IEC 60601-2-47 Edition 2.0 2012-02; IEC 60601-2-49; IEC 60601-2-52;” “IEC 60601-2-39:20181; EN 60601-2-39:2019; GB 9706.239:2021; CSA C22.2 No. 60601-2- 39:2023; Electromyographs and Evoked Response Equipment IEC 60601-2-40:2016; CAN/CSA C22.2 No. 60601-2- 40:2017; EN 6”

Labs
4
Primary AB
A2LA4 labs

Accredited Labs

About ISO/IEC 17025 in United States

American Association for Laboratory Accreditation (A2LA) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in United States.

ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.

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