JUVAPLUS SA - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

41 results · 56ms · Sources: EU EUDAMED, US FDA

Filter by

Basic UDI-DI 14 Device 14 FDA UDI 8 Authorized representative 2 Certificate 1 Importer 1 Manufacturer 1 + More Filters

Country

Switzerland 30 United States 8 France 1 Germany 1 Poland 1 + More Countries

Manufacturer

Juvaplus Sa 32 Beyes Dental Canada Inc 1 Cranberry International Sdn. Bhd. 1 Foshan Anle Medical Apparatus Co., Ltd. 1 Hart Biologicals Ltd. 1 Light Instruments Ltd. 1 Oxy Prem Ag 1 Polydentia Sa 1 Shinhung Co., Ltd. 1 Medmix Switzerland Ag 1 + More Manufacturers

Competent Authority

De/Ca39, Regierungspräsidium Freiburg Referat 25 31 Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 1 The Office For Registration Of Medicinal Products, Medical Devices And Biocidal Products 1 + More Competent Authorities

Kind

Sterilization 6 Active 1 Administering Medicine 1 + More Kinds

Classification

Eu Md Class 1 16 Eu Md Class 2a 12 + More Classifications

Notified Body

Dnv Product Assurance As 14 + More Notified Bodies

Regulation

Eu Mdr 16 Eu Mdd 12 Us FDA 8 + More Regulations

Authorized Representative

Eu Swiss Med Gmb H 30 Juvaplus Europe 30 + More Authorized Representatives

Certificate Type

Mdd Annex Ii (Excluding Section 4) 14 + More Certificate Types

Status

On The Market 14 + More Statuses

MARKU DENTAL Spółka z ograniczoną odpowiedzialnością

🇵🇱 Poland·8 Manufacturers

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.