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BEUDAMED

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4,381 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

Filter by

FDA Pre-Market Approval 4k FDA classification 34 FDA 510(k) 10 + More Filters

Country

United States 4k + More Countries

Classification

FDA Class 3 4k + More Classifications

FDA FEI Number

1317628 4k 1610287 3k 1119279 3k 3002807944 3k 3012236936 3k 3015456951 2k 1038833 2k 3002957101 2k 3004161528 2k 1000121259 2k 1037089 2k 1211998 2k 2246552 2k 3013022457 2k 1119421 2k 2648035 2k 3002807314 2k 3002808262 2k 3004651700 2k 3007530141 2k + More FDA FEI Numbers

Regulation

Us FDA 4k + More Regulations

FDA Registration Number

1313525 4k 1610287 3k 1119279 3k 9681121 3k 3012236936 3k 3015456951 2k 1038833 2k 1064514 2k 9710098 2k 2529709 2k 1037089 2k 1211998 2k 2246552 2k 3013022457 2k 1119421 2k 2648035 2k 3002807314 2k 3007530141 2k 3010155661 2k 3017636737 2k + More FDA Registration Numbers

FDA K Number

K771933 1 K842504 1 K842892 1 K844895 1 K860205 1 K881459 1 K893829 1 K913626 1 K914311 1 K922590 1 + More FDA K Numbers

Ring, Endocapsular

FDA classification

FDA Class 3 ·Ring, Endocapsular

<1 …216 217 218 219 220 >

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

BEUDAMED

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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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