3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-1 testing. From the accredited scope text: “IEC 60601-2-1:2020 IEC 60601-2-1:2009 IEC 60601-2-1:2009/AMD1:2014 Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency sur” “IEC 60601-2-1; IEC 60601-2-1 Edition 4.0 2020-10; IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03; IEC 60601-2-3; IEC 60601-2-4; IEC 60601-2-4 Edition 3.1 2018-02 Consolidated Version; IEC 60601-2-5;” “IEC 60601-2-1 (Section 201.17) 1; ANSI C63.27:2017 Basic Standards (Conducted; Radiated – 9 kHz to 40 GHz; 3m / 10m site) CFR 47, FCC Part 15, Part B (using ANSI C63.4:2014); CFR 47, FCC Part 18 (usin”
Suite A Irvine, CA, US
IEC 60601-2-1:2020 IEC 60601-2-1:2009 IEC 60601-2-1:2009/AMD1:2014 Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency
Kentwood, MI, US
IEC 60601-2-1; IEC 60601-2-1 Edition 4.0 2020-10; IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03; IEC 60601-2-3; IEC 60601-2-4; IEC 60601-2-4 Edition 3.1 2018-02 Consolidated Version; IEC 60601-2-5; IEC 60601-2-5 Edition 3.0 2009-
Middlefield, OH, US
IEC 60601-2-1 (Section 201.17) 1; ANSI C63.27:2017 Basic Standards (Conducted; Radiated – 9 kHz to 40 GHz; 3m / 10m site) CFR 47, FCC Part 15, Part B (using ANSI C63.4:2014); CFR 47, FCC Part 18 (using MP-5:1986); CFR 47, FCC P
This page is a fixed slice of the register: every IEC 60601-2-1 scope we hold for United States. Search narrows it further by city, accreditation body, or a term from the scope text itself.
Search labs in United StatesAmerican 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.