IEC 60601-2-30 Accredited Testing Labs Worldwide

12 accredited laboratories in 5 countries hold IEC 60601-2-30 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs

Countries

Available in 5 Countries

Japan

2 labs

Canada

1 lab

China

1 lab

Top matrices for IEC 60601-2-30

Medical equipment, electrical safety and EMC

1 lab

Sample labs

TUV SUD Japan Ltd. Yonezawa Testing Center (EMC Lab)

Yamagata, JP

IEC 60601-2-30; EN 60601-2-30; IEC 80601-2-30 (clause 202 only); IEC 60601-2-37; EN 60601-2-37; JIS T 0601-2-37; IEC 60601-2-37:2007 + AMD1:2015 (clause 202 only); IEC 60601-2-39; EN IEC 60601-2-39; JIS T 0601-2-39 (clause 202 only)

QPS Evaluation Services

Toronto, ON, CA

IEC 60601-2-30; IEC 60601-2-32; IEC 60601-2-33; IEC 60601-2-34; IEC 60601-2-36; IEC 60601-2-4; IEC 60601-2-40

Element Materials Technology Irvine

Irvine, CA, US

IEC 60601-2-30; EN 60601-2-30; 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

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

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-2-30 (Excluding Cl 36); IEC 60601-2-31 (Excluding Cl 201.17, 202); IEC 60601-2-336 (Excluding Cl 201.17, 202); IEC 60601-2-34 (Excluding Cl 201.17, 202); IEC 60601-2-35 (Excluding Cl 201.17, 202); IEC 60601-2-36 (Excluding Cl

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

IEC 60601-2-30 : 1999-12⊗ Medical electrical equipment - Part 2-30: Particular requirement s for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment IEC 60601-2-31 : 2020-01

CSA Group Bayern

Plattling, DE

IEC 60601-2-30 : 1999-12 ⊗ Medical electrical equipment - Part 2-30: Particul ar requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment CAN/CSA-C22.2 NO. 60601-

Intertek Testing Services NA

Duluth, GA, US

IEC 60601-2-30; IEC 60601-2-32; IEC 60601-2-34; IEC 60601-2-35 (Ed. 2 + Am 1) (excluding cl 201.8.8.4.101); IEC 60601-2-36; IEC 60601-2-37 (Ed. 2 + Am 1, Ed. 3) (excluding cl 201.12); IEC 60601-2-38; IEC 60601-2-40 (Ed. 1, Ed. 2, Ed.

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-2-30:1999); Deutsche Fassung EN 60601-2-30:2000 VDE 0750-2-30 (2000-12)⊗ DIN EN IEC 60601-2-31 : 2021-07 Medizinische elektrische Geräte - Teil 2-31: Besondere Anforderungen an die Basissicherheit einschließlich der wesentl

Eurofins Product Service

Reichenwalde, DE

IEC 60601-2-30:1999); German version EN 60601-2-30:2000 VDE 0750-2-30 (2000-12) ⊗ DIN EN IEC 80601-2-49:2020-10 Medical electrical eq uipment - Part 2-49: Particular requirements for the basic safety and essential performance of multif

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-2-30 (Automatic Cycling Non-Invasive Blood Pressure Monitoring Equipment); EN/IEC 60601-2-34 (Direct Blood Pressure Monitoring Equipment); EN/IEC 60601-2-35 (Blankets, Pads, and Mattresses Intended for Heating); EN/IEC 60601-2

TUV SUD Japan

Tokyo, JP

IEC 60601-2-30:1999 (Excluding Sections 201.106, 202.6.2.102); EN 60601-2-30:2000 (Excluding Sections 201.106, 202.6.2.102); IEC 80601-2-30:2009 (Excluding Sections 201.106, 202.6.2.102); IEC 80601-2-30:2009 + A1:2013 (Excluding Sectio

TUV SUD America

San Diego, CA, US

IEC 60601-2-30 (2Ed 1999); EN 60601-2-30 (2000); CAN/CSA-C22.2 No. 60601-2-30 (2002+R:2006+R2011); IEC 60601-2-31 Edition 2.1 2011-09; IEC 60601-2-31 (1Ed 1994 + A1:1998, 2Ed 2008+A1:2011); IEC 60601-2-31:2020; EN 60601-2-31 (200