Tracker - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

2,041 results · 49ms · Sources: EU EUDAMED, US FDA

Filter by

FDA UDI 2k FDA registration 404 FDA 510(k) 49 Device 27 Basic UDI-DI 19 FDA Pre-Market Approval 17 + More Filters

Country

United States 2k Pakistan 103 France 21 Germany 17 China 8 South Korea 6 Malaysia 5 Austria 2 Canada 2 India 2 Japan 2 Switzerland 2 United Kingdom 2 Iceland 1 Italy 1 Mexico 1 Netherlands 1 Singapore 1 Thailand 1 Türkiye 1 + More Countries

Manufacturer

Biosynex 16 Philips Ultrasound Llc 14 Localite Gmb H 5 Brainlab Ag 2 Fiagon Gmb H 2 Awesome Health 1 Gold Standard Diagnostics Kassel Gmb H 1 Mesa Ideas Srl 1 Mod Jaw 1 Si Bone, Inc. 1 Sejoy Biomedical Co., Ltd. 1 Thomson Software Solutions Ltd 1 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 17 Ministry Of Health, Welfare And Sports 14 De/Ca21 Bezirksregierung Köln Dezernat 24 5 De/Ca304 Marktüberwachung Medizinprodukte Bayern 2 De/Ca76 Landesamt Für Arbeitsschutz, Verbraucherschutz Und Gesundheit Abt. Gesundheit Dezernat G4 2 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 1 De/Ca30 Regierungspräsidium Kassel Dezernat 55 Medizinprodukte Und Produktsicherheitsrecht 1 Danish Medicines Agency, Pharmacovigilance & Medical Devices 1 Health Products Regulatory Authority, Medical Devices Department 1 Malta Medicines Authority 1 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 1 + More Competent Authorities

Kind

Animal Tissues 9 Professional Testing 9 Reagent 9 Kit 8 Microbial Substances 8 Active 5 New Device 4 Software 2 Near Patient Testing 1 Reusable 1 Self Testing 1 Sterilization 1 + More Kinds

Classification

FDA Class 2 48 Eu Md Class 1 18 Eu Ivd Class B 16 FDA Class 3 13 Eu Md Class 2a 10 FDA Class 1 3 Eu Ivd General 1 Eu Ivd Self Testing 1 FDA Unclassified 1 + More Classifications

Notified Body

Tüv Rheinland Lga Products Gmb H 1 Tüv Süd Product Service Gmb H 1 + More Notified Bodies

FDA FEI Number

1720747 220 1000347621 103 2011171 29 1220477 27 1450662 26 1721676 26 3001236277 25 1000136269 24 3000206435 24 3008114965 24 3016678045 24 1000138054 23 1018470 23 1000306431 22 1526534 22 2183744 22 3013557562 22 1928237 21 2528981 21 1047843 20 + More FDA FEI Numbers

Regulation

Us FDA 2k Eu Mdr 28 Eu Ivdr 16 Eu Ivdd 2 + More Regulations

Authorized Representative

Philips Medical Systems Nederland B.V. 14 Advena Limited 1 Icon (Lr) Limited 1 Shanghai International Holding Corp. Gmb H(europe) 1 Sigma Tech Nordic Ap S 1 + More Authorized Representatives

FDA Registration Number

1720747 220 3007597038 103 2011171 29 1220477 27 1450662 26 1721676 26 1649518 25 2030624 24 2244478 24 3008114965 24 3016678045 24 1018470 23 1319639 23 1526534 22 2029275 22 2183744 22 3013557562 22 1928237 21 2528981 21 1047843 20 + More FDA Registration Numbers

Certificate Type

Ivdd Annex Iv (Excluding Sections 4, 6) 2 + More Certificate Types

Status

On The Market 27 + More Statuses

iQ Curved ILM Forceps

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

<1 …99 100 101 102 103 >

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.