IEC 60601-2-5 Accredited Testing Labs Worldwide

31 accredited laboratories in 9 countries hold IEC 60601-2-5 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs

Countries

Top matrix

Medical equipment, electrical safety and EMC

3 labs

Available in 9 Countries

China

5 labs

Japan

2 labs

Canada

2 labs

Taiwan

2 labs

Netherlands

1 lab

Italy

1 lab

South Korea

1 lab

Top matrices for IEC 60601-2-5

Medical equipment, electrical safety and EMC

3 labs

Sample labs

E & C Testlab GmbH (Engineering & Certification Testlab GmbH)

Trossingen, DE

IEC 60601-2-5 : 2009-07 Medical electrical equipment - Part 2-5: Particular requirements for basic safety and essential performance of ultrasonic physiotherapy equipment IEC 60601-2-6 : 2012-04 Medical electrical equipment - Part 2-6: P

QPS Evaluation Services

Toronto, ON, CA

IEC 60601-2-52; IEC 60601-2-57; IEC 60601-2-5; IEC 60601-2-7; IEC 80601-2-69; UL 187; UL 60601-1 (excluding Clauses 36, 37, 40, 41, and 44.7) Miscellaneous Electrical Equipment CAN/CSA B149.3; CAN/CSA-C22.2 No. 102; CAN/CSA-

Intertek Japan K.K.

Tokyo, JP

IEC 60601-2-5; IEC 60601-2-5: Edition 3.0 2009-07; IEC 60601-2-18; EN 60601-2-18; IEC 60601-2-18: Edition 3.0 2009-08; IEC 60601-2-28 (Ed 2, Ed 3); IEC 60601-2-28 Edition 3.0 2017-06;

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

Guangzhou, Guangdong, CN

IEC 60601-2-5; EN 60601-2-5; CSA C22.2 NO. 60601-2-5 Dental Device Related Testing: ISO 7494-1; EN ISO 7494-1; ISO 7494-2; EN ISO 7494-2; ISO 9680; EN ISO 9680; ISO 10650; EN ISO 10650; ISO 9168; EN ISO 9168; ISO 18397; EN ISO 18397

TÜV Technische Überwachung Hessen GmbH EMV-Labor

Kassel, DE

IEC 60601-2-5:2000); Deutsche Fassung EN 60601-2-5:2000 VDE 0750-2-5:2001-12 DIN EN 60601-2-6:2017-10 Medizinische elektrische Geräte - Teil 2-6: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkma

Element Materials Technology Irvine

Irvine, CA, US

IEC 60601-2-57 Edition 1.0 2011-01; IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57, (excluding 201.6.1.102, 201.10.103, 201.13.1.101); IEC 60601-2-62:2013; EN 60601-2-62:2015; CAN/CSA-C22.2 No. 60601-2-62:15, (excludi

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-2-5:2009); Deutsche Fassung EN 60601-2-5:2015 DIN EN 60601-2-6 : 2017-10 Medizinische elektrische Geräte - Teil 2-6: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Mikrowellen-Thera

TÜV Rheinland Japan Ltd. Yokohama Laboratories Global Technology Assessment Center

Japan, DE

IEC 60601-2-5:2015 VDE 0750-2-5: 2016-08 Medical electrical equipment - Part 2 -5: ParDcular requirements for basic safety and essenDal performance of ultrasonic physiotherapy equipment. A Product Safety IEC 60601 -2-7:1998 EN 60

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

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-2-50 (Cl 201.17, 202); ANSI/AAMI/IEC 80601-2-30 (Cl 201.17, 202); ANSI/AAMI/IEC 80601-2-35 (Cl 201.17, 202); ANSI/AAMI MP 80601-2-49 (Cl 201.11.6.5, 201.17, 202); ANSI/AAMI/IEC 80601-2-58 (Cl 201.17, 202); ANSI/AAMI/IEC 8060

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

IEC 60601-2-5:2009); Deutsche Fassung EN 60601-2-5:2015

TUV SUD Canada

Gormley, ON, CA

IEC 60601-2-5: Edition 3.0 2009-07; IEC 60601-2-6 Edition 2.1 2016-04; IEC 60601-2-8 Edition 2.1 b:2015; IEC 60601-2-10 Edition 2.1 2016-04; ISO 80601-2-12 Second edition 2020-02; ISO 80601-2-12 Third edition 2023-11

CSA Group Bayern

Plattling, DE

IEC 60601-2-5:2009); Deutsche Fassung EN 60601-2-5:2015 VDE 0750-2-5:2016-08 DIN EN 60601-2-5 : 2001-12 ⊗ - Medizinische elektrische Geräte - Teil 2-5: Besondere Festlegungen für die Sicherheit von Ultraschall-Physiotherapiegeräten (I

Shenzhen Huatongwei International Inspection Co.,

Shenzhen, CN

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 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-25 Edition 2.0 2011-10 3-105

MedTech Testing Solution Co.,

New Taipei City, TW

IEC 60601-2-5; EN 60601-2-5; BS EN 60601-2-5; CAN/CSA C22.2 No. 60601-2-5; AS 60601.2.5 Transcutaneous electrical nerve stimulators IEC 60601-2-10; EN 60601-2-10; BS EN 60601-2-10; CAN/CSA-C22.2 No. 60601-2-10; AS 60601.2.10;

UL LLC

Novi, MI, US

IEC 60601-2-5: Edition 3.0 2009-07 (clause 201.17 only) 12-205 IEC 60601-2-6 Edition 2.1 2016-04 (clause 202 only) 6-423 IEC 60601-2-10 Edition 2.1 2016-04 (clause 202 only) 17-16 IEC 60601-2-16 Edition 5.0 2018-4 (clause 202 only) 9-121

SGS Taiwan

Taoyuan City, TW

IEC 60601-2-5; EN 60601-2-5; CAN/CSA-C22.2 No. 60601-2-5 High-voltage generators of diagnostic X-ray generators IEC 60601-2-7; EN 60601-2-7; CAN/CSA-C22.2 No. 60601-2-7; JIS Z 4751-2-7 Nerve and muscle stimulators IEC 60601-2-10; E

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-2-5:2009); Deutsche Fassung EN 60601-2-5:2015; VDE 0750-2-5:2016-08 DIN EN 60601-2-5 : 2001-120 - Medizinische elektrische Geräte - Teil 2-5: Besondere Festlegungen für die Sicherheit von Ultraschall-Physiotherapiegeräten (IEC

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

Shenzhen, Guangdong, CN

IEC 60601-2-5; EN 60601-2-5; CAN/CSA-C22.2 No. 60601-2-5; IEC 60601-2-22; EN IEC 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22; IEC 60601-2-24; EN 60601-2-24; CAN/CSA-C22.2 No. 60601-2-24; IEC 60601-2-25; EN 60601-2-25; ANSI/AAM

Intertek Testing Services NA

Kentwood, MI, US

IEC 60601-2-5; IEC 60601-2-5 Edition 3.0 2009-07 (The above standards exclude Clause 201.10.102 Unwanted Ultrasound Radiation, Clause 201.12 Accuracy of controls and instruments and protection against hazardous outputs);

F2 Labs

Middlefield, OH, US

IEC 60601-2-5: Edition 3.0 2009-07 (Section(s) 201.17/202) 1; ANSI AAMI IEC 60601-2-50 Edition 2.1 2016-04; (Section(s) 201.17/202) 1; IEC 60601-2-50 Edition 3.0 2020-09 (Section(s) 201.17/202) 1; IEC 60601-2-52 Edition 1.1 2015-03 CONS

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

Straubing, DE

IEC 60601-2-5 : 2009-07 IEC 60601-2-6 : 2012-04 IEC 60601-2-10 : 2012-06 DAkkS Deutsche Akkreditierungsstelle Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-2-5 Edition 3.0 2009-07 12-205 IEC 60601-2-6 Edition 2.1 2016-04 6-423 IEC 60601-2-8 Edition 2.1 b:2015 12-301 IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-11 Edition 3.0 2013-01 12-255 IEC 60601-2-16 Edition 5.0 201

PHOENIX TESTLAB

Blomberg, DE

IEC 60601-2-5:2000); Deutsche Fassung EN 60601-2-5:2000 DIN EN 60601-2-21 : 2017-09 Medizinische elektrisch e Geräte - Teil 2-21: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Säuglingsw

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

TÜV Rheinland Korea Ltd. Test Center, Safety of Electrical Appliances and Ergonomics

Republic Of, DE

The testing laboratory is permitted, without being required to inform and obtain prior approval from DAkkS, to use standards or equivalent testing methods listed here with different issue dates. The testing laboratory maintains a current

SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

IEC 60601-2-50 - Infant warmer DIN EN 60601-2-21 IEC 60601-2-21 - Ultrasound physiotherapy devices DIN EN 60601-2-5 IEC 60601-2-5 - Devices for extracorporeally induced lithotripsy DIN EN 60601-2-36 IEC 60601-2-36

Sigma Scientific Services

Sunrise, FL, US

IEC 60601-2-5 Edition 3.0 2009-07 12-205 IEC 60601-2-62 Edition 1.0 2013-07 12-281

SHENZHEN STS TEST SERVICES CO.,LTD.

Shenzhen, CN

Test Technology: Test Method(s): Product Safety (Cont’d) AS/NZS 60669.1 (excluding: 22.5, 25); IEC/EN 60669-2-1 (excluding: 22.5, 25); BS

White Lab S.r.l. - Test'ing

Falconara Marittima, IT

IEC 60601-2-5:2009 _ Par 04 - Prescrizioni generali/General requirements, Par 05 - Prescrizioni generali per le prove sugli apparecchi EM/General requirements for testing ME Equipment, Par 06 - Classificazione degli apparecchi EM e dei si

TUV SUD Japan

Tokyo, JP

IEC 60601-2-5:2000 (Only Sections, 50, 51.5, 51.104); EN 60601-2-5:2000 (Only Sections 35, 50, 51.5, 51.104); JIS T 0601-2-5:2005 (Only Sections 35, 50, 51.5, 51.104); IEC 60601-2-5:2009 (Only Sections 201.10.102, 201.12.1, 201.12.4.4

Kiwa Nederland

RIJSWIJK ZH, NL

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