IEC 60601-1-12 Accredited Testing Labs Worldwide

37 accredited laboratories in 8 countries hold IEC 60601-1-12 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs

Countries

Available in 8 Countries

China

12 labs

Canada

2 labs

United Kingdom

2 labs

Taiwan

2 labs

Japan

1 lab

South Korea

1 lab

Top matrices for IEC 60601-1-12

Medical equipment, electrical safety and EMC

Sample labs

TÜV SÜD Certification and Testing (China) Co., Ltd. Guangzhou Branch

China, DE

IEC 60601-1-12; IEC 60601-1-12 Edition 1.0 2014-06; IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-12; ANSI AAMI IEC 60601-1-12:2016 [Including AMD 1:2021]; CSA C22.2 No. 60601-1-12; EN 60606-1-12

QPS Evaluation Services

Toronto, ON, CA

IEC 60601-1-12; IEC 60601-1-3; IEC 60601-1-4; IEC 60601-1-8; IEC 60601-2-10; IEC 60601-2-18; IEC 60601-2-2; IEC 60601-2-23; IEC 60601-2-25; IEC 60601-2-26; IEC 60601-2-27; IEC 60601-2-30; IEC 60601-2-32; IEC 60601-2-33; IEC 60

SGS-CSTC Standards Technical Services Co., Ltd. Guangzhou Branch

Guangzhou, Guangdong, CN

IEC 60601-1-12; EN 60601-1-12; ANSI/AAMI/IEC 60601-1-12; CAN/CSA-C22.2 No. 60601-1-12; EN 1789; IEC 62304; EN 62304; ISO 20417; EN ISO 20417; ISO 80369-2; ISO 18190 (except clasue 6.1.2, 6.1.3) Ultrasound Equipment: IEC 62359; EN 6

TÜV Technische Überwachung Hessen GmbH EMV-Labor

Kassel, DE

DIN EN 60601-1-11:2021-12 Medizinische elektrische Geräte - Teil 1-11: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale - Ergänzungsnorm: Anforderungen an medizinische elektrische Geräte und med

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-1-12:2014); Deutsche Fassung EN 60601-1-12:2015 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz-Chirurgiegeräten (IEC 60601-2

SGS-CSTC Standards Technical Services (Shanghai) Co.,

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-1-12 (Cl 6.2, 8.1, 10.1); ANSI/AAMI/IEC 60601-2-2 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-4 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-16 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-19 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-20 (Cl

TUV SUD America - Auburn Hills

Auburn Hills, MI, US

IEC 60601-1-12 Section 4.2.2 Environmental Vibration* (Including Environmental Vibration) SAE/USCAR-2; GMW3172; GMW3431; MIL-STD-810, Method 514; IEC 60601-1-11 Section 10; IEC 60068-2-64; IEC 60601-1-12 Section 10; IEC 60068-2

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

This document is a translation. The definitive version is the original German annex to the accreditation certificate. Geräten und in medizinischen elektrischen Systemen (IEC 60601-1- 8:2006 + A1:2012); Deutsche Fassung EN 60601 -1-8:2007

TUV SUD Canada

Gormley, ON, CA

IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-12:2016 [Including AMD 1:2021]; IEC 60601-2-2 Edition 6.0 2017-03; ANSI AAMI IEC 60601-2-2:2017; IEC 60601-2-5: Edition 3.0 2009-07; IEC 60601-2-6 Edition 2

CSA Group Bayern

Plattling, DE

IEC 60601-1-12:2014); Deutsche Fassung EN 60601- 1-12:2015 DIN EN 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfreque

Intertek Testing Services NA

Duluth, GA, US

Tests: Standard(s) 2: Laboratory / Process Control / Test Equipment Products (excluding UV Radiation, Flammable Liquids, Cathode ray tubes test) (continued) UL 61010-2-040:2021, Ed. 3; UL 61010-2-051:2015, Ed. 3; UL 61010-2-051:

Eurofins Electrical Testing Service (Shenzhen) Co.,

Shenzhen City, Guangdong, CN

IEC 60601-1-12; CSA-C22.2 No. 60601-1-12 Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators IEC/EN 60601-2-10 Part 2-18: Particular requirements for the basic safety a

Shenzhen Huatongwei International Inspection Co.,

Shenzhen, CN

IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION 19-39 IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-5 Edition 3.0 2009-07 12-205 IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 6060

MedTech Testing Solution Co.,

New Taipei City, TW

IEC 60601-1-12; EN 60601-1-12; BS EN 60601-1-12; CAN/CSA C22.2 No. 60601-1-12; AS IEC 60601.1.12; ANSI AAMI IEC 60601-1-12 High frequency surgical equipment and high frequency surgical accessories IEC 60601-2-2; EN IEC 60601-2

Eurofins Electrical Testing Service (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-12; EN 60601-1-12; ANSI AAMI IEC 60601-1-12; CSA-C22.2 No. 60601-1-12

Shenzhen CTL Testing Technology Co.,

Shenzhen, CN

IEC 60601-1-12; EN 60601-1-12; ANSI AAMI IEC 60601-1-12 Medical electrical equipment –Part 2-60: Particular requirements for the basic safety and essential performanceof dental equipment IEC 80601-2-60; EN IEC 80601-2-60 Medica

SGS Taiwan

Taoyuan City, TW

IEC 60601-1-12; EN 60601-1-12; ANSI/AAMI/IEC 60601-1-12; CAN/CSA-C22.2 No. 60601-1-12 High frequency surgical equipment and accessories IEC 60601-2-2; EN IEC 60601-2-2; ANSI/AAMI 60601- 2-2; CSA C22.2 NO. 60601-2-2

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-1-12:2014); Deutsche Fassung EN 60601-1-12:2015 DIN EN IEC 60601-2-1 : 2022-12 Medizinische elektrische Geräte - Teil 2-1: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Elektron

Eurofins Product Service

Reichenwalde, DE

IEC 60601-1-12:2014 + A1:2020); German version EN 60601-1-12:2015 + A1:2020 VDE 0750-1-12:2022-02 DIN EN 60601-1-12 : 2016-01 ⊗ - Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performan

Element Materials Technology Warwick

Warwick, GB

IEC 60601-1-12:2014 BS EN 60601-1-12:2015 IEC 60601-1-12:2014 + A1:2020 EN 60601-1-12:2015 + A1:2020 Excluding:- 11: EMC Testing F Only Clause 8.3 (ingress protection) B Safety of Emergency Medica

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch

Shenzhen, Guangdong, CN

IEC 60601-1-12; EN 60601-1-12; ANSI/AAMI/IEC 60601-1-12; CAN/CSA-C22.2 No. 60601-1-12; IEC 60601-2-10; EN 60601-2-10; CAN/CSA-C22.2 No.60601-2-10; ISO 80601-2-12; EN ISO 80601-2-12; CAN/CSA-C22.2 No. 80601-2-12; ISO 80601-2-13

DEKRA Testing and Certification (Shanghai) Ltd., Guangzhou Branch

Guangzhou, CN

IEC 60601-1-12; EN 60601-1-12; ANSI/AAMI/IEC 60601-1-12; CAN/CSA-C22.2 No. 60601-1-12 Medical electrical equipment – Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-12; EN 60601-1-12; DIN EN 60601-1-12; VDE 0750-1-12; IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-12:2016 [Including AMD 1:2021] Medical electrical equipment – Part 2-2: Particul

Intertek Testing Services NA

Kentwood, MI, US

IEC 60601-1-12; IEC 60601-1-12 Edition 1.1 2020-07 Consolidated Version (The above standards exclude Clauses 10.1.2 Requirements for mechanical strength for FIXED or PERMANENTLY INSTALLED MEE intended for use in a road amb

TÜV SÜD Product Service GmbH PS-SL-EMC / PS-SL-ENV-STR

Straubing, DE

IEC 60601-1-12:2014); Deutsche Fassung EN 60601-1-12:2015 DIN EN IEC 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequen

Black Forest Testlab OHG

Löffingen, DE

IEC 60601-1-12:2014 + A1:2020); Deutsche Fassung EN 60601-1-12:2015 + A1:2020 VDE 0750-1-12:2022-02 DIN EN IEC 60601-2-2 : 2018-12 ⊗ Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-1-12 (Equipment for EMS use Environments); EN/IEC 60601-2-2 (High Frequency Surgical Equipment); EN/IEC 60601-2-4 (Cardiac Defibrillators); EN/IEC 60601-2-5 (Ultrasonic Physiotherapy Equipment); EN/IEC 60601-2-8 (Therapeutic X

cetecom advanced

Saarbrücken, DE

IEC 60601-1-12:2014); Deutsche Fassung EN 60601-1-12:2015 DIN EN 60601-2-4:2021-09 Medizinische elektrische G eräte - Teil 2-4: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Defibrillato

SGS Korea Co., Ltd. (Gunpo Laboratory)

Gunpo-si, KR

3 Exclusions Table Standard Clause Measurement/testing IEC 60601-1 9.5 Expelled parts Hazard 9.5.2 Cathode ray tubes. 9.7.5 Pressure vessels 11.2.2 ME Equipment and ME systems used in conjunction with. 11.4 ME Equipment and ME System

DEKRA Testing and Certification (Suzhou) Co.,

Suzhou, Jiangsu Province, CN

IEC 60601-1-12 Medical electrical equipment – Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators IEC/EN 60601-2-4; CAN/CSA-C22.2 NO. 60601-2-4; ANSI/AAMI/IEC 60601-2-4 Me

Element Materials Technology - Hull

Kingston upon Hull, GB

IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-12:2016 [Including AMD 1:2021]; CSA CAN/CSA-C22.2 No. 60601-1-12:15 + A1:21 Medical electrical equipment — Part 1-12; IEC 60601-1-11:2015; IEC 60601-2-24:2

SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

IEC 60601-1-12 Environmental simulation tests information provided by the manufacturer Check for compliance - Instructions for use/accompanyin g documents

Medical Equipment Compliance Associates, LLC.

Oak Creek, WI, US

IEC 60601-1-12; IEC 60601-1-12:2014 + A1:20201; ANSI/AAMI/IEC 60601-1-12; ANSI/AAMI/IEC 60601-1-12:2016 + A1:20211; CAN/CSA C22.2 No. 60601-1- 12; EN 60601-1-12; IEC 60601-1, Edition 3.2 Particular Standards High Frequency Sur

Bay Area Compliance

Sunnyvale, CA, US

IEC 60601-1-12 (2014); IEC 60601-2-37 (2015); IEC TR 60601-4-2 (2016); CAN/CSA C22.2 No. 60601-1 (2008); ANSI AAMI ES60601-1 (2005/(R)2012) and A1:2012, C1:2009/(R)2012 and A2:2010/(R) 2012 (Consolidated Text) [Incl. AMD2:2021]; EN 60

TUV Rheinland (Shenzhen) Co.,

Shenzhen, CN

IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI/AAMI IEC 60601-1-12:2016 [Including AMD 1:2021] 19-39 IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION 12-336 IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-1

TUV SUD Japan

Tokyo, JP

IEC 60601-1-12:2014 (Excluding sections 10.1.2, 10.1.3, 10.1.4); IEC 60601-1-12:2014/AMD1:2020(Excluding sections 10.1.2, 10.1.3, 10.1.4);

TUV SUD America

San Diego, CA, US

IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION 19-39 IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-19 Edition 3.0 2020-09 6-461 IEC 60601-2-20 Edition 3.0 2020-09 6-462 IEC 60601