PRODONT-HOLLIGER - BEUDAMED

BEUDAMED

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1,261 results · 69ms · Sources: EU EUDAMED, US FDA

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Device 1k FDA UDI 74 Basic UDI-DI 45 FDA registration 20 Certificate 1 Manufacturer 1 + More Filters

Country

France 1k United States 74 + More Countries

Manufacturer

Prodont Holliger 1k + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 1k + More Competent Authorities

Kind

Sterilization 1k Measuring Function 32 + More Kinds

Classification

Eu Md Class 1 1k + More Classifications

Notified Body

Kiwa Cermet Italia S.P.A. 66 + More Notified Bodies

FDA FEI Number

3002807935 20 + More FDA FEI Numbers

Regulation

Eu Mdr 1k Us FDA 94 Eu Mdd 64 + More Regulations

FDA Registration Number

9611899 20 + More FDA Registration Numbers

Certificate Type

Mdd Annex V 66 + More Certificate Types

Status

On The Market 1k No Longer On The Market 32 + More Statuses

med31465

MDD Annex V·Prodont-Holliger·KIWA CERMET ITALIA S.P.A.·32 Basic UDI-DIs

<1 …60 61 62 63 64 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

A better medical device search engine by OpenRegulatory.

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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.

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