IEC 60601-2-40 Accredited Testing Labs Worldwide
22 accredited laboratories in 9 countries hold IEC 60601-2-40 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 9 Countries
Top matrices for IEC 60601-2-40
Sample labs
IEC 60601-2-40 Third edition 2024-12; IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION; IEC 60601-2-43 Edition 3.0 2022-12; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-47 Edition 2.0 2012-02; ANSI AAMI IEC 60601-2-47:2012/(R)2
IEC 60601-2-40
IEC 60601-2-40:2016-08 Medical electrical equipment - Part 2-40: Particular requirements for the safety and essential performance of electromyo graphs and evoked response equipment IEC 60601-2-47:2012-02 Medical electrical equipment - Pa
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 60601-2-40:2016); Deutsche Fassung EN 60601-2-40:2019 VDE 0750-2-40:2019-04 DIN EN 60601-2-40 : 1998-12 ⊗ Medizinische elektrische Geräte - Teil 2-40: Besondere Festlegungen für die Sicherheit von Elektromyographen und Geräten für
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 + Am 1); IEC 80
IEC 60601-2-40; EN IEC 60601-2-40
IEC 60601-2-40; EN 60601-2-40; CAN/CSA-C22.2 No. 60601-2-40 Operating tables IEC 60601-2-46; EN IEC 60601-2-46; CAN/CSA C22.2 NO. 60601-2-46 Ambulatory electrocardiographic systems IEC 60601-2-47; EN 60601-2-47; ANSI/AAMI 606
IEC 60601-2-40:2016); Deutsche Fassung EN 60601-2-40:2019 DIN EN 60601-2-40 : 1998-12⊗ - Medizinische elektrische Geräte - Teil 2-40: Besondere Festlegungen für die Sicherheit von Elektro- myographen und Geräten für evozierte Potentiale
IEC 60601-2-40 : 2016-08 Medical electrical equipme nt - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment IEC 60601-2-40 : 1998-02 ⊗ - Medical electrical
IEC 60601-2-40:2016 Excluding:- 201.12.4.104: limitation of visual stimulator output 202: EMC testing F Only Clause 201.12.4.6 (acoustic pressure) G Safety of non-laser light source equipment for t
IEC 60601-2-40; EN 60601-2-40; CAN/CSA-C22.2 No. 60601-2-40; ISO 80601-2-55; EN ISO 80601-2-55; CAN/CSA-C22.2 No. 80601-2-55; ISO 80601-2-56; EN ISO 80601-2-56; IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57;
IEC 60601-2-40; EN 60601-2-40; CAN/CSA-C22.2 No. 60601-2-40 Medical electrical equipment – Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis IEC 606
IEC 60601-2-40 / IS 13450-2-40: 2018 Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitors IEC 80601-2-49 / IS 13450-2-49 Medical electr
Deutsche Akkreditierungsstelle DIN EN IEC 60601-2-39 : 2020-05 Medizinische elektrische Geräte - Teil 2-39: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Peritoneal-Dialyse-Geräten (IEC 6060
IEC 60601-2-40 (Electromyographs and Evoked Response Equipment); EN/IEC 60601-2-41 (Surgical Luminaires and Luminaires for Diagnosis); EN/IEC 60601-2-43 (X-ray Equipment for Interventional Procedures); EN/IEC 60601-2-44 (X-ray Equipment
according DIN EN ISO/IEC 17025:2018 Valid from : 03.05.2024 Date of issue : 09.05.2025 Page 30 of 42 This document is a translation. The definitive version is the original German annex to the accreditation certificate. DIN E
IEC 60601-2-40:2016; CAN/CSA C22.2 No. 60601-2- 40:2017; EN 60601-2-40:2019; YY 9706.240:2021; Multiparameter Patient Monitoring Equipment IEC 80601-2-49:2018; EN IEC 60601-2-49:2019; Safety of Medical Beds IEC 60601-2-52:2009 +
IEC 60601-2-40 Medical electrical equipment - Part 2-63: Particular requirements for the basic safety and essential performance of dental extra- oral X-ray equipment IEC 60601-2-63 Medical electrical equipment - Part 2-65: Particular
IEC 60601-2-40 Geräte zur Überwachung von vitalen Parametern Prüfung der Einhaltung der allgemeinen und besonderen Festlegungen - Elektrokardiographen DIN EN 60601 -2-25 IEC 60601-2-25 DIN EN 60601-2-27 IEC 60601-2-27 Ster
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 60601-2-40 (1Ed 1998, 2Ed 2016); EN 60601-2-40 (1998, 2017); CAN/CSA-C22.2 No. 60601-2-40 (2001+R:2005+R:2009, 2017); IEC 60601-2-41 (1Ed 2000; 2Ed 2009+A1:2013); EN 60601-2-41 (2009+A11:2011); CAN/CSA-C22.2 No. 60601-2-41