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

IEC 60601-2-27 Accredited Testing Labs in United States

9 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60601-2-27 testing. From the accredited scope text: “IEC 60601-2-27 Edition 3.0 2011-03 (clause 202 only) 3-126 IEC 60601-2-31 Edition 2.1 2011-09 (clause 202 only) 3-102 IEC 60601-2-33 Ed. 3.2 b:2015 (clause 202 only) 12-295 IEC 60601-2-34 Edition 3.0” “IEC 60601-2-27 (Electrocardiographic Monitoring Equipment); EN/IEC 60601-2-28 (X-ray Tube Assembly for Medical Diagnostics); IEC 60601-2-30 (Automatic Cycling Non-Invasive Blood Pressure Monitoring Eq” “IEC 60601-2-27:2011(R)2016 1; IEC 60601-2-28 Edition 2.0 2010-03 (Section(s) 201.17/202) 1; IEC 60601-2-28 Edition 3.0 2017-06 (Section(s) 201.17/202) 1; IEC 60601-2-29 Edition 3.0 2008-06 (Section(s)” “IEC 60601-2-27 (Ed. 2, Ed. 3); 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) (excludi”

Labs
9
Primary AB
A2LA9 labs

Accredited Labs

Intertek Testing Services NA

Duluth, GA, US

Scope

IEC 60601-2-27 (Ed. 2, Ed. 3); 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; I

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UL LLC

Novi, MI, US

Scope

IEC 60601-2-27 Edition 3.0 2011-03 (clause 202 only) 3-126 IEC 60601-2-31 Edition 2.1 2011-09 (clause 202 only) 3-102 IEC 60601-2-33 Ed. 3.2 b:2015 (clause 202 only) 12-295 IEC 60601-2-34 Edition 3.0 2011-05 (clause 202 only) 3-115 IEC

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EUROFINS ELECTRICAL AND ELECTRONIC TESTING NA

Suite A Irvine, CA, US

Scope

IEC 60601-2-27: Edition 3.0 2011-03; 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

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Intertek Testing Services NA

Kentwood, MI, US

Scope

IEC 60601-2-27; IEC 60601-2-27 Edition 3.0 2011-03; IEC 60601-2-36; IEC 60601-2-36 Edition 2.0 2014-04; IEC 60601-2-37; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2024-07 (The above standards exclude Clause 201.

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F2 Labs

Middlefield, OH, US

Scope

IEC 60601-2-27:2011(R)2016 1; IEC 60601-2-28 Edition 2.0 2010-03 (Section(s) 201.17/202) 1; IEC 60601-2-28 Edition 3.0 2017-06 (Section(s) 201.17/202) 1; IEC 60601-2-29 Edition 3.0 2008-06 (Section(s) 201.17/202) 1; IEC 60601-2-31 Editi

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TUV Rheinland of North America

Pleasanton, CA, US

Scope

IEC 60601-2-27 (Electrocardiographic Monitoring Equipment); EN/IEC 60601-2-28 (X-ray Tube Assembly for Medical Diagnostics); IEC 60601-2-30 (Automatic Cycling Non-Invasive Blood Pressure Monitoring Equipment); EN/IEC 60601-2-34 (Direct

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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 60601-2-27 3-126 ANSI AAMI IEC 60601-2-27 3-126 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 A

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TUV SUD America

San Diego, CA, US

Scope

IEC 60601-2-27 Edition 3.0 2011-03 3-126 ANSI AAMI IEC 60601-2-27:2011(R)2016 3-126 IEC 60601-2-47 Edition 2.0 2012-02 3-155 ANSI AAMI IEC 60601-2-47:2012/(R)2016 3-155 IEC 60601-2-2 Edition 6.0 2017-03 6-389 ANSI AAMI IEC 60601-2-2:20

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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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