VYGON - BEUDAMED

BEUDAMED

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2,061 results · 36ms · Sources: EU EUDAMED, US FDA

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FDA UDI 2k FDA registration 317 FDA 510(k) 75 Importer 5 Manufacturer 3 Authorized representative 1 FDA Pre-Market Approval 1 System producer 1 + More Filters

Country

United States 2k France 150 Germany 17 Belgium 14 Colombia 14 Portugal 10 Italy 3 Denmark 2 Dominican Republic 1 Ireland 1 Mexico 1 Türkiye 1 + More Countries

Manufacturer

Shenzhen Caremed Medical Technology Co.,Ltd. 2 Tidi Products, Llc. 2 Beijing Konted Medical Technology Co.,Ltd 1 Besmed Health Business Corp. 1 Chemence Medical Inc. 1 Cobes Industries(hefei) Co.,Ltd 1 Gbuk Group 1 Gvs Filter Technology Uk Limited 1 Great Group Medical Co., Ltd. 1 Hb Fuller, Medical Adhesive Technologies 1 Hans Rudolph Inc 1 Health Line International Corp 1 Interrad Medical, Inc. 1 Koo Medical Equipment (Shanghai) Co., Ltd. 1 Luma Clean Llc 1 Nonin Medical, Inc. 1 Oxy Nov Inc. 1 Pharma Sept Medical Products Ltd. 1 Shenzhen Hawk Medical Instrument Co., Ltd. 1 Sino Medical Device Technology Co., Ltd 1 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 3 Danish Medicines Agency, Pharmacovigilance & Medical Devices 2 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 2 De/Ca21 Bezirksregierung Köln Dezernat 24 1 Health Products Regulatory Authority, Medical Devices Department 1 Turkish Medicine And Medical Devices Agency 1 + More Competent Authorities

Classification

FDA Class 2 68 FDA Class 1 7 FDA Class 3 1 + More Classifications

FDA FEI Number

3011237770 125 3009291251 110 1000120555 105 2245270 94 1000138054 60 2011171 58 3013557562 57 1220477 55 3001236905 53 3005747797 53 1018233 50 1000512168 49 1043214 48 3000206435 47 3012307300 47 1820334 46 3003737899 45 3004111573 45 3010041511 44 3005011024 43 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

3011237770 125 1223004 105 8020785 96 2245270 94 1319639 60 2011171 58 3013557562 57 1220477 55 1423537 53 3011137372 53 1018233 50 1061124 49 1043214 48 2030624 47 3012307300 47 1820334 46 3004111573 45 9680794 45 3010041511 44 3005011024 43 + More FDA Registration Numbers

FibreKor Fiber Post Drill

FDA registration

Ormex S. de R.L. de C.V.·1 product·🇲🇽 Mexico

<1 …100 101 102 103 104 >

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

BEUDAMED

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BEUDAMED

Rationale
MDR Notified Bodies
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Tools

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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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