K122845 - BEUDAMED

BEUDAMED

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381 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 334 FDA registration 26 FDA classification 18 FDA UDI 3 + More Filters

Country

United States 368 Canada 3 Mexico 2 Denmark 1 France 1 Germany 1 Greece 1 Israel 1 Japan 1 Spain 1 Switzerland 1 + More Countries

Classification

FDA Class 1 348 FDA Class 2 4 + More Classifications

FDA FEI Number

1000123428 361 1043214 339 3017264244 330 3017633586 330 3006076154 323 3013657868 323 1000123222 322 1000208624 318 3004605321 317 2110420 312 3005273623 308 1417592 307 3010452421 307 1038963 304 2110898 302 3003764610 299 3006513362 299 3006943846 298 3005951403 297 3006227741 297 + More FDA FEI Numbers

Regulation

Us FDA 381 + More Regulations

FDA Registration Number

1122845 361 1043214 339 3017264244 330 3017633586 330 3013657868 323 9616086 323 1123071 322 1060680 318 3004605321 317 2110420 312 3005273623 308 1417592 307 3010452421 307 1038963 304 2110898 302 3003764610 299 3006513362 299 3006943846 298 3005951403 297 3006227741 297 + More FDA Registration Numbers

FDA K Number

K000066 1 K000636 1 K001240 1 K001311 1 K001941 1 K001945 1 K002184 1 K002361 1 K002486 1 K002710 1 K002775 1 K003235 1 K003788 1 K011076 1 K011118 1 K011139 1 K011170 1 K011237 1 K011334 1 K011335 1 + More FDA K Numbers

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone

<1 …16 17 18 19 20 >

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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