3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform ISO 80601-2-80 testing. From the accredited scope text: “ISO 80601-2-80 First edition 2018-07 1-144 1 These methods have been assessed by A2LA according to A2LA’s FDA ASCA Program requirements. Accreditation by A2LA does not imply FDA ASCA-Accreditation. Al” “ISO 80601-2-80 First Edition 2018-07 (Section(s) 201.17/202) 1; IEC 60601-1-2 Edition 4.1 2020-09 CONSOLIDATED VERSION 1; ANSI AAMI IEC 60601-1-2:2014 [Including AMD 1:2021]; IEC TR 60601-4-2 Field Te” “ISO 80601-2-80; ISO 80601-2-80 Second edition 2024-08; ISO 80601-2-80 First edition 2018-07; IEC 62304; IEC 62366; IEC 62366-1; ISO 9919; ISO 8185; IEC 60601-2-47; IEC 60601-2-20; IEC 60601-2-66; IEC”
Duluth, GA, US
ISO 80601-2-80 First edition 2018-07 1-144 1 These methods have been assessed by A2LA according to A2LA’s FDA ASCA Program requirements. Accreditation by A2LA does not imply FDA ASCA-Accreditation. All ASCA-accreditation decisions for
Kentwood, MI, US
ISO 80601-2-80; ISO 80601-2-80 Second edition 2024-08; ISO 80601-2-80 First edition 2018-07; IEC 62304; IEC 62366; IEC 62366-1; ISO 9919; ISO 8185; IEC 60601-2-47; IEC 60601-2-20; IEC 60601-2-66; IEC 80601-2-35; IEC 60601-2-83; IE
Middlefield, OH, US
ISO 80601-2-80 First Edition 2018-07 (Section(s) 201.17/202) 1; IEC 60601-1-2 Edition 4.1 2020-09 CONSOLIDATED VERSION 1; ANSI AAMI IEC 60601-1-2:2014 [Including AMD 1:2021]; IEC TR 60601-4-2 Field Testing – In situ Methods 2 Emiss
This page is a fixed slice of the register: every ISO 80601-2-80 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.