3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-28 testing. From the accredited scope text: “IEC 60601-2-28 (X-ray Tube Assembly for Medical Diagnostics); IEC 60601-2-30 (Automatic Cycling Non-Invasive Blood Pressure Monitoring Equipment); EN/IEC 60601-2-34 (Direct Blood Pressure Monitoring E” “IEC 60601-2-28 Edition 2.0 2010-03 (Section(s) 201.17/202) 1; IEC 60601-2-28 Edition 3.0 2017-06 (Section(s) 201.17/202) 1; IEC 60601-2-29 Edition 3.0 2008-06 (Section(s) 201.17/202) 1; IEC 60601-2-31” “IEC 60601-2-28 Edition 3.0 2017-06 12-309 IEC 60601-2-33 Ed. 3.2 b:2015 12-295 IEC 60601-2-33 Edition 4.0 2022-08 12-347 IEC 60601-2-34 Edition 3.0 2011-05 3-115 IEC 60601-2-35 Edition 2.0 2020-09 6-4”
Duluth, GA, US
IEC 60601-2-28 Edition 3.0 2017-06 12-309 IEC 60601-2-33 Ed. 3.2 b:2015 12-295 IEC 60601-2-33 Edition 4.0 2022-08 12-347 IEC 60601-2-34 Edition 3.0 2011-05 3-115 IEC 60601-2-35 Edition 2.0 2020-09 6-483 IEC 60601-2-37 Edition 2.1 2015
Middlefield, OH, US
IEC 60601-2-28 Edition 2.0 2010-03 (Section(s) 201.17/202) 1; IEC 60601-2-28 Edition 3.0 2017-06 (Section(s) 201.17/202) 1; IEC 60601-2-29 Edition 3.0 2008-06 (Section(s) 201.17/202) 1; IEC 60601-2-31 Edition 2.1 2011-09 (Section(s) 201.
Pleasanton, CA, US
IEC 60601-2-28 (X-ray Tube Assembly for Medical Diagnostics); IEC 60601-2-30 (Automatic Cycling Non-Invasive Blood Pressure Monitoring Equipment); EN/IEC 60601-2-34 (Direct Blood Pressure Monitoring Equipment); EN/IEC 60601-2-35 (Blanke
This page is a fixed slice of the register: every IEC 60601-2-28 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.