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BEUDAMED

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41 results · 16ms · Sources: EU EUDAMED, US FDA

Filters Classification: Eu Md Class 2a ×

Filter by

Basic UDI-DI 23 Device 18 + More Filters

Country

China 22 Türkiye 14 Belgium 2 Italy 2 + More Countries

Manufacturer

Shanghai Pz Medical Technology Co., Ltd. 22 Sayan Tıbbi Aletler Paz. San. Ve Tic. Ltd. şti. 14 General Topics Srl 2 Hasa Optix 2 + More Manufacturers

Competent Authority

De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 22 Turkish Medicine And Medical Devices Agency 14 Federal Agency For Medicines And Health Products / / Health Products Division 2 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 2 + More Competent Authorities

Kind

Reusable 17 Active 11 Measuring Function 11 Sterilization 7 Administering Medicine 1 + More Kinds

Classification

Eu Md Class 2a 41 + More Classifications

Notified Body

Szutest Uygunluk Değerlendirme A.ş. 14 Istituto Superiore Di Sanita' 2 Mtic Inter Cert S.R.L. 2 + More Notified Bodies

Regulation

Eu Mdr 23 Eu Mdd 18 + More Regulations

Authorized Representative

Shanghai International Holding Corp. Gmb H(europe) 22 + More Authorized Representatives

Certificate Type

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

Status

On The Market 18 + More Statuses

Sets de soins cutanés et de plaies

EU MDR · Eu Md Class 2a ·88 devices

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

BEUDAMED

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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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