IEC 60601-2-38 Accredited Testing Labs Worldwide
13 accredited laboratories in 5 countries hold IEC 60601-2-38 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 5 Countries
Top matrices for IEC 60601-2-38
Sample labs
IEC 60601-2-38; IEC 60601-2-41; IEC 60601-2-43 (Ed 2, Ed 2.1); IEC 60601-2-43 Edition 3.0 2022-12; IEC 60601-2-44; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-46; IEC 60601-2-52; IEC 60601-2-52 Edition 1.1 2015-03 CONSOLIDATED
IEC 60601-2-38:1996-10⊗ Medical electrical equipment - Part 2-38: Particular requirements for the safety of electrically operated hospital beds + Amendment 1:1999-12⊗ IEC 60601-2-40:2016-08 Medical electrical equipment - Part 2-40: Parti
IEC 60601-2-38:1996 + A1:1999); Deutsche Fassung EN 60601-2-38:1996 + A1:2000 Medizinische elektrische Geräte - Teil 2-43: Besondere Festlegungen für die Sicherheit und wesentlichen Leistungsmerkmale von Röntgeneinrichtungen für interventio
Test Technology: Test Method(s)2,3: Medical Equipment (cont.) EN 60601-2-336 (Excluding Cl 201.17, 202); EN 60601-2-34 (Excluding Cl 201.17
IEC 60601-2-38:1996 + A1:1999); Deutsche Fassung EN 60601-2-38:1996 + A1:2000 VDE 0750 : 2001-07 ⊗ DIN EN 60601-2-40 : 2019-04 Medizinische elektrische Geräte - Teil 2-40: Besondere Festlegungen für die Sicherheit einschließlich der we
IEC 60601-2-38; IEC 60601-2-40 (Ed. 1, Ed. 2, Ed. 3); IEC 60601-2-41 (Ed. 2 + Am 1, Ed. 3); 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
IEC 60601-2-38; IEC 60601-2-39; IEC 60601-2-39 Edition 3.0 2018-04; IEC 60601-2-44; IEC 60601-2-44 Edition 3.2 2016; 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 60601-2-5
IEC 60601-2-38 (Electrically Operated Hospital Beds); EN/IEC 60601-2-39 (Peritoneal Dialysis Equipment); EN/IEC 60601-2-40 (Electromyographs and Evoked Response Equipment); EN/IEC 60601-2-41 (Surgical Luminaires and Luminaires for Diagno
IEC 60601-2-38:1996 + A1:1999); Deutsche Fassung EN 60601-2-38:1996 + A1:2000 VDE 0750 : 2001-07 ⊗ DIN EN 60601-2-50 : 2017-09 ⊗ Medizinische elektrische Geräte - Teil 2-50: Beson dere Festlegungen für die Sicherheit einschließlich de
IEC 60601-2-38:1996 + A1:1999); German version EN 60601-2-38:1996 + A1:2000 DIN EN 60601-2-40 : 2019-04 Medical electrical equ ipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyograp
Department Standard / in house procedure / Version Title of standard or in-house procedure (deviations / modifications of standard) Test area / reductions Medical Equipment # DIN EN 60601 -2-37:2016 VDE 0750-2-37:2016 Medica
Normative document: EN ISO/IEC 17025:2017 Registration number: L 015 of Kiwa Nederland B.V. Kiwa FSS Testing This annex is valid from: 29-01-2026 to 01-09-2028 Replaces annex dated: 28-01-2026 Dutch Accreditation Council RvA
IEC 60601-2-38 (1Ed 1996+A1:1999); EN 60601-2-38 (1996+A1:2000); CAN/CSA-C22.2 No. 60601-2-38 (2003+Gen Ins1:2006+R:2007); CSA CAN/CSA-C22.2 No. 60601-2-52 (2011+ R:2016+A1:2014) IEC 60601-2-40 (1Ed 1998, 2Ed 2016); EN 60601-2