NJF - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

1,341 results · 26ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

Filter by

FDA 510(k) 1k + More Filters

Country

United States 1k Germany 1 Greece 1 + More Countries

Classification

FDA Class 1 1k + More Classifications

FDA FEI Number

3012494290 433 3012421607 399 1417592 360 3013557562 303 3015550354 290 3001236905 284 3007208013 278 3006198300 273 2432235 268 3002806559 265 2517506 259 3008875470 256 1827821 247 1043214 246 3002750084 244 3014683120 235 1832216 233 3010131137 233 2183301 231 1000136573 230 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3012494290 433 3012421607 399 1417592 360 3013557562 303 3015550354 290 1423537 284 3007208013 278 3006198300 273 2432235 268 9610126 265 2517506 259 2024980 256 1827821 247 1043214 246 1836161 244 3014683120 235 1832216 233 3010131137 233 2183301 231 1319681 230 + More FDA Registration Numbers

UPACS VERSION 1.7

FDA Class 1 ·Radiology

<1 …64 65 66 67 68 >

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

API Documentation
API Dashboard
EUDAMED API on GitHub
Imprint

BEUDAMED

Rationale
MDR Notified Bodies
MDR Competent Authorities

OpenRegulatory

OpenRegulatory
Formwork eQMS Software
Digital Health Jobs
EUDAMED Budget Monitor
eidel.io

Tools

510(k) Predicate Finder
Product Code Directory
510(k) Review Times
21 CFR Regulations
NB Comparison

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.

© 2026 OpenReg GmbH. All rights reserved.