3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-46 testing. From the accredited scope text: “IEC 60601-2-46 (Operating Tables); EN/IEC 60601-2-47 (Ambulatory Electrocardiographic Systems); EN/IEC 60601-2-49 (Multifunction Patient Monitoring Equipment); EN/IEC 60601-2-50 (Infant Phototherapy E” “IEC 60601-2-46 (Ed. 3, Ed. 4); IEC 60601-2-49 (Ed. 1, Ed.2); IEC 60601-2-50 (Ed. 2 + Am1, Ed. 3 + Am1); IEC 60601-2-51; IEC 60601-2-52 (Ed. 1 + Am 1); IEC 80601-2-26 (Ed. 1 + Am 1); IEC 80601-2-30 (Ed” “IEC 60601-2-46; IEC 60601-2-47; IEC 60601-2-47 Edition 2.0 2012-02; IEC 60601-2-49; IEC 60601-2-52; IEC 60601-2-52 Edition 1.0 2009-12; IEC 60601-2-52 Edition 1.1 2015-03 Consolidated Version; IEC 606”
Duluth, GA, US
IEC 60601-2-46 (Ed. 3, Ed. 4); IEC 60601-2-49 (Ed. 1, Ed.2); IEC 60601-2-50 (Ed. 2 + Am1, Ed. 3 + Am1); IEC 60601-2-51; IEC 60601-2-52 (Ed. 1 + Am 1); IEC 80601-2-26 (Ed. 1 + Am 1); IEC 80601-2-30 (Ed. 1.1, Ed. 2.0); ANSI/AAMI/IEC 80
Kentwood, MI, US
IEC 60601-2-46; IEC 60601-2-47; IEC 60601-2-47 Edition 2.0 2012-02; IEC 60601-2-49; IEC 60601-2-52; IEC 60601-2-52 Edition 1.0 2009-12; IEC 60601-2-52 Edition 1.1 2015-03 Consolidated Version; IEC 60601-2-66; IEC 60601-2-68;
Pleasanton, CA, US
IEC 60601-2-46 (Operating Tables); EN/IEC 60601-2-47 (Ambulatory Electrocardiographic Systems); EN/IEC 60601-2-49 (Multifunction Patient Monitoring Equipment); EN/IEC 60601-2-50 (Infant Phototherapy Equipment); EN/IEC 60601-2-51 (Record
This page is a fixed slice of the register: every IEC 60601-2-46 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.