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Registers collected 2026-08-22.See collection dates
ISO/IEC 17025 directory

IEC 60601-2-34 Accredited Testing Labs in United States

9 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-34 testing. From the accredited scope text: “IEC 60601-2-34 Edition 3.0 2011-05 (clause 202 only) 3-115 IEC 60601-2-36 Edition 2.0 2014-04 (clause 202 only) 9-119 IEC 60601-2-37 Edition 2.1 2015 (clauses 201.17, 202 only) 12-293 IEC 60601-2-44 E” “IEC 60601-2-34 (Direct Blood Pressure Monitoring Equipment); EN/IEC 60601-2-35 (Blankets, Pads, and Mattresses Intended for Heating); EN/IEC 60601-2-36 (Equipment for extra-corporeally induced lithotr” “IEC 60601-2-34 Edition 3.0 2011-05 (Section(s) 201.17/202) 1; IEC 60601-2-36 Edition 2.0 2014-04 (Section(s) 201.17/202) 1; IEC 60601-2-37 Edition 2.1 2015 (Section(s) 201.17/202) 1; IEC 60601-2-37 Ed” “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”

Labs
9
Primary AB
A2LA9 labs

Accredited Labs

Intertek Testing Services NA

Duluth, GA, US

Scope

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. 3); IEC 60601-2-41 (Ed. 2 + Am

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UL LLC

Novi, MI, US

Scope

IEC 60601-2-34 Edition 3.0 2011-05 (clause 202 only) 3-115 IEC 60601-2-36 Edition 2.0 2014-04 (clause 202 only) 9-119 IEC 60601-2-37 Edition 2.1 2015 (clauses 201.17, 202 only) 12-293 IEC 60601-2-44 Edition 3.2: 2016 (clause 202 only) 12

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EUROFINS ELECTRICAL AND ELECTRONIC TESTING NA

Suite A Irvine, CA, US

Scope

IEC 60601-2-34: Edition 3.0 2011-05; IEC 60601-2-52: Edition 1.0 2009-12; IEC 60601-2-57: Edition 1.0 2011-01; IEC 61010-1: Edition 3.1 2017-01; IEC/ANSI/AAMI 60601-1-12; IEC/EN/UL 61010-2-030; CSA C22.2 No. 61010-2-030 Enclosure In

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Intertek Testing Services NA

Kentwood, MI, US

Scope

IEC 60601-2-34; IEC 60601-2-34 Edition 4.0 2024-10; IEC 60601-2-34 Edition 3.0 2011-05; IEC 60601-2-41; IEC 60601-2-46; IEC 60601-2-49; IEC 80601-2-49; IEC 80601-2-49 Edition 1.1 2024-09 CONSOLIDATED VERSION; IEC 60601-2-50

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F2 Labs

Middlefield, OH, US

Scope

IEC 60601-2-34 Edition 3.0 2011-05 (Section(s) 201.17/202) 1; IEC 60601-2-36 Edition 2.0 2014-04 (Section(s) 201.17/202) 1; IEC 60601-2-37 Edition 2.1 2015 (Section(s) 201.17/202) 1; IEC 60601-2-37 Edition 3.0 2024-07; IEC 60601-2-43

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TUV Rheinland of North America

Pleasanton, CA, US

Scope

IEC 60601-2-34 (Direct Blood Pressure Monitoring Equipment); EN/IEC 60601-2-35 (Blankets, Pads, and Mattresses Intended for Heating); EN/IEC 60601-2-36 (Equipment for extra-corporeally induced lithotripsy); EN/IEC 60601-2-37 (Ultrasoni

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UL Verification Services

Fremont, CA, US

Scope

(A2LA Certificate No. 0751.05) Revised 03/02/2026 Page 3 of 10 Test Technology: Test Method(s) 1, 2: EMC Medical (continued) IEC/EN 60601-2-25 (cl. 202 only); IEC/EN 60601-2-27 (cl. 202 only); IEC/EN 60601-2-31 (cl. 202 only); IEC/EN

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Medical Equipment Compliance Associates, LLC.

Oak Creek, WI, US

Scope

IEC 60601-2-34 3-115 IEC 60601-2-36 9-119 IEC 60601-2-37 12-293 IEC 60601-2-47 3-155 ANSI AAMI IEC 60601-2-47 3-155 IEC 61010-1 19-34 ANSI/UL 61010-1 19-41 IEC 80601-2-30 3-123 ANSI AAMI IEC 80601-2-30 3-123 ISO 80601-2-55 1-140 I

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TUV SUD America

San Diego, CA, US

Scope

IEC 60601-2-34 Edition 3.0 2011-05 3-115 ANSI AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:2009/(R)2012 & A2:2010/(R)2012 (Cons. Text) [Incl. AMD2:2021 19-46 IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION 19-49 ANSI/AAMI HA60601-1-1

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About ISO/IEC 17025 in United States

American Association for Laboratory Accreditation (A2LA) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in United States.

ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.

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