Amann Girrbach AG - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

1,641 results · 103ms · Sources: EU EUDAMED, US FDA

Filter by

FDA UDI 1k Device 234 FDA registration 37 Basic UDI-DI 6 FDA 510(k) 3 Manufacturer 1 + More Filters

Country

United States 1k Austria 271 + More Countries

Manufacturer

Amann Girrbach Ag 240 + More Manufacturers

Competent Authority

Austrian National Public Health Institute 241 + More Competent Authorities

Kind

Cmr Substance 7 Sterilization 5 + More Kinds

Classification

Eu Md Class 2a 215 Eu Md Class 1 25 FDA Class 2 2 FDA Unclassified 1 + More Classifications

FDA FEI Number

3030515618 30 3005942449 13 2433919 3 2523320 3 3003215343 3 3003719498 3 3004491043 3 3005904906 3 3008320092 3 3008347275 3 3009432160 3 3009482106 3 3009727738 3 3011649314 3 3013551048 3 3022068322 3 1000293792 2 1036212 2 1219645 2 1410097 2 + More FDA FEI Numbers

Regulation

Us FDA 1k Eu Mdr 240 + More Regulations

FDA Registration Number

3030515618 30 3005942449 13 1064812 3 2433919 3 2523320 3 3004491043 3 3005904906 3 3008320092 3 3008347275 3 3009432160 3 3009482106 3 3009727738 3 3011649314 3 3013551048 3 3022068322 3 9614977 3 1000625496 2 1036212 2 1219645 2 1410097 2 + More FDA Registration Numbers

Status

On The Market 234 + More Statuses

Zirkonoxidkeramik Klasse 5

EU MDR · Eu Md Class 2a ·Amann Girrbach AG·180 devices

<1 …79 80 81 82 83 >

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.