GSK - BEUDAMED

BEUDAMED

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201 results · 20ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 171 FDA Pre-Market Approval 27 FDA classification 3 + More Filters

Country

United States 141 South Korea 16 China 10 Israel 6 Slovakia 5 Türkiye 5 Denmark 4 Germany 4 Canada 2 Finland 2 Sweden 2 Switzerland 2 Australia 1 Hong Kong 1 + More Countries

Classification

FDA Class 2 201 + More Classifications

FDA FEI Number

2124215 93 2183744 93 1000306431 91 3002095335 87 3002807111 87 3000126629 84 3009973336 84 3012104670 83 3015997711 83 3005210579 82 3009077524 82 3005334138 81 3006950086 81 3012536737 81 3015309643 81 3033589330 81 2221819 80 2648727 80 2939520 80 3000957797 80 + More FDA FEI Numbers

Regulation

Us FDA 201 + More Regulations

FDA Registration Number

2124215 93 2183744 93 2029275 91 2134265 87 3005941719 86 3000126629 84 3009973336 84 3012104670 83 3015997711 83 3005210579 82 3009077524 82 3005334138 81 3006950086 81 3012536737 81 3015309643 81 3033589330 81 1066270 80 2221819 80 2648727 80 2939520 80 + More FDA Registration Numbers

FDA K Number

K002067 1 K002742 1 K003122 1 K011865 1 K013943 1 K021517 1 K033738 1 K070795 1 K080670 1 K081805 1 K092733 1 K102674 1 K102704 1 K110631 1 K112915 1 K113644 1 K122721 1 K141615 1 K142103 1 K150157 1 + More FDA K Numbers

Computer, Blood-Pressure

FDA classification

FDA Class 2 ·Computer, Blood-Pressure

<1 …7 8 9 10 11 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

A better medical device search engine by OpenRegulatory.

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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