Intertek Testing Services NA
Kentwood, MI, US
IEC 62040-1-1; IEC 62040-1-2; EN 62040-2:2006; IEC 62040-2:2005; UL 1778; UL 60950-22 (excluding Dust) Medical IEC 60601-1; EN 60601-1; IEC 60601-1 Edition 3.2 2020-08 Consolidated Version (The a
3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 62040-1 testing. From the accredited scope text: “IEC 62040-1 (1Ed 2008+A1:2013); IEC 62040-1:2017+A1:2021+ A2:2022; EN 62040-1 (2008+A1:2013); EN IEC 62040-1:2019/A1:2023 ITAV IEC 62368-1 (1Ed 2010; 2Ed 2014; 3Ed 2018; 4Ed 2023); EN 62368-1 (2Ed 201” “IEC 62040-1-1; IEC 62040-1-2; EN 62040-2:2006; IEC 62040-2:2005; UL 1778; UL 60950-22 (excluding Dust) Medical IEC 60601-1; EN 60601-1; IEC 60601-1 Edition 3.2 2020-08 Consolidated Version (The above”
Kentwood, MI, US
IEC 62040-1-1; IEC 62040-1-2; EN 62040-2:2006; IEC 62040-2:2005; UL 1778; UL 60950-22 (excluding Dust) Medical IEC 60601-1; EN 60601-1; IEC 60601-1 Edition 3.2 2020-08 Consolidated Version (The a
Pleasanton, CA, US
Test Description: Test Method 1: Measurement (excluding clauses detailed in Table #4 below) 3 (cont.) IEC/EN/UL/CSA 61010-2-091(Cabinet X-ray systems, [non-medical]); EN/IEC/CSA 61010-2-101 (In vitro diagnostic (IVD) Medical Equipme
San Diego, CA, US
IEC 62040-1 (1Ed 2008+A1:2013); IEC 62040-1:2017+A1:2021+ A2:2022; EN 62040-1 (2008+A1:2013); EN IEC 62040-1:2019/A1:2023 ITAV IEC 62368-1 (1Ed 2010; 2Ed 2014; 3Ed 2018; 4Ed 2023); EN 62368-1 (2Ed 2014 + A11:2017); EN IEC 62368-1
This page is a fixed slice of the register: every IEC 62040-1 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.