Ori Inc - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

481 results · 60ms · Sources: EU EUDAMED, US FDA

Filter by

FDA UDI 262 FDA registration 121 FDA 510(k) 94 Authorized representative 2 FDA Pre-Market Approval 1 Importer 1 + More Filters

Country

United States 477 Germany 3 Australia 1 + More Countries

Manufacturer

Changshu Kangbao Medical Appliance Factory 2 Wingderm Electro Optics Ltd. 2 Yiwu Ori Power Medtech Co.,Ltd. 2 Shenzhen Calibeur Industries Co., Ltd. 1 Amcaremed Technology Co., Limited 1 Amido (Beijing) Enterprises Limited 1 Anhui Jica Care Equipment Co.,Ltd 1 Anhui Remed Medical Products Co., Ltd. 1 Ankiya Bio Tec Co., Ltd. 1 Apostar Medical (Shanghai)limited. 1 Arsci Biomedical Inc. 1 Aso Llc 1 Acare Medical Science Co., Ltd. 1 Accu Pulse Medical Device (Suzhou) Ltd. 1 Accu Target Medi Pharma (Shanghai) Co., Ltd. 1 Affacare Medical (Beijing) Co., Ltd. 1 Ailex Technology Group Co., Ltd. 1 Alfa Medtech (Shanghai) Co., Ltd. 1 Allmed Medical Products Co.,Ltd 1 American Safety Power Tool Pvt Ltd 1 + More Manufacturers

Competent Authority

De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 1 De/Ca304 Marktüberwachung Medizinprodukte Bayern 1 De/Ca32 Landesamt Für Soziales, Jugend Und Versorgung 1 + More Competent Authorities

Classification

FDA Class 2 92 FDA Class 1 1 FDA Unclassified 1 + More Classifications

FDA FEI Number

2011171 86 1000138054 81 3000126629 78 3009077524 78 1000219637 72 3008496839 72 3002808382 71 3010326005 71 1000158431 70 1000571342 70 2183553 70 3001814065 70 3002807880 70 3002808157 70 3003377038 70 3004531751 70 3004754211 70 3004929307 70 3004977335 70 3005049692 70 + More FDA FEI Numbers

Regulation

Us FDA 478 + More Regulations

FDA Registration Number

2011171 86 1319639 81 3000126629 78 3009077524 78 1058584 72 3008496839 72 3010326005 71 9614698 71 1529041 70 1835830 70 1932898 70 2183553 70 3002808157 70 3003768277 70 3004531751 70 3004754211 70 3004929307 70 3004977335 70 3005049692 70 3005326970 70 + More FDA Registration Numbers

Lohmann & Rauscher International GmbH & Co. KG

🇩🇪 Germany·23 Manufacturers

<1 …21 22 23 24 25 >

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.