KZS - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

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

Filters Classification: FDA Class 2 ×

Filter by

FDA 510(k) 381 + More Filters

Country

United States 361 Canada 10 China 3 Denmark 2 Hungary 2 South Korea 2 Taiwan 1 + More Countries

Classification

FDA Class 2 381 + More Classifications

FDA FEI Number

1417592 120 3013557562 119 3012494290 109 1220477 96 3000126629 96 3012307300 94 1000306431 93 3005747797 92 2011171 91 3001236277 90 3003076831 86 3002807391 85 3026408938 85 3000215273 82 3004111573 82 3018094310 81 1450662 80 3018783526 79 3023272766 79 3001236905 78 + More FDA FEI Numbers

Regulation

Us FDA 381 + More Regulations

FDA Registration Number

1417592 120 3013557562 119 3012494290 109 1220477 96 3000126629 96 3012307300 94 2029275 93 3011137372 92 2011171 91 1649518 90 2032112 86 3026408938 85 9610849 85 1423662 82 3004111573 82 3018094310 81 1450662 80 3018783526 79 3023272766 79 1423537 78 + More FDA Registration Numbers

BIPRO MODEL SDS-CB200

FDA Class 2 ·Gastroenterology, Urology

<1 …16 17 18 19 20 >

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.