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

IEC 60601-2-23 Accredited Testing Labs in United States

5 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-23 testing. From the accredited scope text: “IEC 60601-2-23 Edition 3.0 2011-02 (clause 202 only) 1-87 IEC 60601-2-25 Edition 2.0 2011-10 (clause 202 only) 3-105 IEC 60601-2-27 Edition 3.0 2011-03 (clause 202 only) 3-126 IEC 60601-2-31 Edition 2” “IEC 60601-2-23 (Transcutaneous Partial Pressure Monitoring Equipment); EN/IEC 60601-2-24 (Infusion Pumps and Controllers); EN/IEC 60601-2-25 (Electrocardiographs); EN/IEC 60601-2-26 (Electroencephalog” “IEC 60601-2-23 Edition 3.0 2011-02 (Section(s) 201.17/202) 1; IEC 60601-2-25 Edition 2.0 2011-10 1; ANSI AAMI IEC 60601-2-25:2011/(R)2016 1; ANSI AAMI IEC 60601-2-25 Edition 2.0 2011-10 (Section(s) 20”

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This page is a fixed slice of the register: every IEC 60601-2-23 scope we hold for United States. Search narrows it further by city, accreditation body, or a term from the scope text itself.

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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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