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BEUDAMED

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41 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 31 FDA 510(k) 10 + More Filters

Country

United States 41 + More Countries

Classification

FDA Class 3 41 + More Classifications

FDA FEI Number

2124215 25 1450662 24 3001092088 24 3002124543 24 3003428886 24 3005579300 24 3009088444 24 3013070673 24 1000127185 10 1000140026 10 1000148701 10 1000305720 10 1000524572 10 1218058 10 1220908 10 1317188 10 1720929 10 1921846 10 1930027 10 2112020 10 + More FDA FEI Numbers

Regulation

Us FDA 41 + More Regulations

FDA Registration Number

2124215 25 1450662 24 3002124543 24 3005579300 24 3009088444 24 3013070673 24 8022247 24 9710358 24 1218058 10 1219103 10 1220908 10 1223925 10 1317188 10 1320894 10 1423537 10 1423662 10 1720929 10 1921846 10 1930027 10 2112020 10 + More FDA Registration Numbers

PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602

FDA Class 3 ·Cardiovascular

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

BEUDAMED

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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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