ECT - BEUDAMED

BEUDAMED

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4,821 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: Eu Md Class 2b ×

Filter by

Device 3k Basic UDI-DI 2k + More Filters

Country

France 3k United States 1k Switzerland 329 China 310 Australia 48 Japan 43 Italy 26 Israel 24 South Korea 20 Malaysia 8 Netherlands 8 Denmark 5 Türkiye 3 India 2 + More Countries

Manufacturer

Neuro France Implants 790 S.M.A.I.O 654 Cambridge Interventional Llc 636 Deltex 574 X Os S.A. 228 Datex Ohmeda Inc. 184 Ortho Cape 164 Eurosilicone Sas 104 Shenzhen Antmed Co., Ltd 102 Gaz Purs Et Fluides 96 Laboratoires Urgo 80 Dongguan Queen Med Equipment Mfg Co Ltd 66 Regen Lab Sa 62 Carestream Dental Llc 54 Ellex Medical Pty Ltd 46 Eurospine Sarl 42 Tht Bio Science 42 Ge Medical Systems Information Technologies, Inc. 40 Shenzhen Witleaf Medical Electronics Co., Ltd 34 Inosystems 33 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 4k De/Ca09 Staatliches Gewerbeaufsichtsamt Hannover 636 De/Ca22 Bezirksregierung Münster 299 Health Products Regulatory Authority, Medical Devices Department 56 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 26 Ministry Of Health, Welfare And Sports 8 Danish Medicines Agency, Pharmacovigilance & Medical Devices 5 Finnish Medicines Agency, Supervision And Licences, Medical Device Unit 3 Turkish Medicine And Medical Devices Agency 3 De/Ca304 Marktüberwachung Medizinprodukte Bayern 1 Federal Agency For Medicines And Health Products / / Health Products Division 1 + More Competent Authorities

Kind

Single Use 2k Implantable 1k Sterilization 1k Sterile 936 Active 734 Orthopedic 492 Administering Medicine 136 Measuring Function 75 Cmr Substance 32 Latex 29 Software 24 Medicinal Product 16 Reusable 11 Animal Tissues 1 Endocrine Disruptor 1 + More Kinds

Classification

Eu Md Class 2b 5k + More Classifications

Notified Body

Gmed Sas 2k Ente Certificazione Macchine Srl 670 Dqs Medizinprodukte Gmb H 574 Sgs Belgium Nv 326 Bsi Group The Netherlands B.V. 180 Tüv Rheinland Lga Products Gmb H 176 Ht Cert (Health Technology Certification Ltd) 166 Tüv Süd Product Service Gmb H 90 Dnv Medcert Gmb H 80 Therapeutic Goods Administration 30 Polskie Centrum Badan I Certyfikacji S.A. 16 Kiwa Cermet Italia S.P.A. 14 Dekra Certification B.V. 12 Mtic Inter Cert S.R.L. 8 Schweizerische Vereinigung Für Qualitäts Und Managementsysteme 8 Udem Uluslararasi Belgelendirme Denetim Egitim Merkezi San. Ve Tic. A.ş. 8 Imq Istituto Italiano Del Marchio Di Qualità S.P.A. 6 Dnv Product Assurance As 5 Tuv Rheinland Italia Srl 4 Institut Pro Testováni A Certifikaci, A. S. (Institute For Testing And Certification) Merged With Ex Nb 1390 2 + More Notified Bodies

Regulation

Eu Mdd 4k Eu Mdr 667 + More Regulations

Authorized Representative

Mdss Gmb H 642 Ge Medical Systems Scs 297 Med Net Ec Rep Gmb H 281 Sas Isocèle Conseil 228 Ge Healthcare Finland Oy 184 Med Net Ec Rep C I Ib Gmb H 135 Regen Lab France 62 Trophy 54 E C Rep Limited 50 Sagami Europe Sas 35 Medi Mark Europe Sarl. 34 Zug Medical Systems 34 Caliceos 32 Med Net Ec Rep Iii Gmb H 24 Med Net Ec Rep I Ib Gmb H 20 Infomed Sas 16 Spectrum Dynamics Medical France Sas 14 Advena Limited 11 Nidek Sa 11 Wellkang Ltd 9 + More Authorized Representatives

Certificate Type

Mdd Annex Ii (Excluding Section 4) 4k Mdd Annex Ii Section 4 43 Mdd Annex Iii 2 + More Certificate Types

Status

On The Market 3k No Longer On The Market 31 Not Intended For Eu Market 23 + More Statuses

ARCEOLE SF6

EU MDD · Eu Md Class 2b ·ARCADOPHTA·1 device

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

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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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