K243757 - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

2,262 results · 44ms · Sources: EU EUDAMED, US FDA

Filter by

FDA 510(k) 2k FDA registration 28 FDA classification 27 FDA UDI 1 + More Filters

Country

United States 2k China 77 Germany 46 Japan 38 United Kingdom 24 South Korea 23 France 22 Denmark 20 Italy 19 Israel 17 Switzerland 13 Taiwan 12 Canada 9 Sweden 7 Austria 5 Netherlands 4 Australia 3 Hong Kong 1 Monaco 1 Singapore 1 + More Countries

Classification

FDA Class 2 2k FDA Class 1 301 FDA Unclassified 34 + More Classifications

FDA FEI Number

2243757 2k 3011050570 2k 2020550 2k 3002808268 2k 3007475226 2k 3012322232 2k 3014342096 2k 3010707607 2k 3002808001 2k 3006546082 2k 3012494290 2k 3013557562 1k 1221826 1k 3004111573 1k 2183744 1k 3002681132 1k 3013298431 1k 3024021261 1k 3013247477 1k 2936485 1k + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

2243757 2k 3011050570 2k 2020550 2k 3010202439 2k 3012322232 2k 3014342096 2k 9610617 2k 3010707607 2k 9611102 2k 3006546082 2k 3012494290 2k 3013557562 1k 1221826 1k 3004111573 1k 2183744 1k 1650907 1k 3013298431 1k 3024021261 1k 3013247477 1k 2936485 1k + More FDA Registration Numbers

FDA K Number

Den150057 1 K000046 1 K000048 1 K000144 1 K000153 1 K000197 1 K000198 1 K000438 1 K000456 1 K000510 1 K000598 1 K000673 1 K000677 1 K000691 1 K000715 1 K000747 1 K000846 1 K000905 1 K001136 1 K001226 1 + More FDA K Numbers

Syringe, Piston

FDA classification

FDA Class 2 ·Syringe, Piston

Forceps

FDA classification

FDA Class 1 ·Forceps

<1 …110 111 112 113 114 >

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.