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5,721 results · 41ms · Sources: EU EUDAMED, US FDA

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FDA UDI 5k FDA registration 148 Device 65 Basic UDI-DI 59 FDA 510(k) 48 FDA Pre-Market Approval 31 Manufacturer 9 Certificate 6 FDA classification 6 Authorized representative 4 Importer 4 System producer 1 + More Filters

Country

United States 5k China 63 Germany 31 France 20 Japan 9 South Korea 8 Türkiye 8 Italy 7 India 6 Canada 5 Finland 5 Poland 5 Hungary 4 Sweden 4 United Kingdom 4 Mexico 3 Netherlands 3 Spain 3 Taiwan 3 Australia 2 + More Countries

Manufacturer

The Yes Yes Company Ltd 24 Ff Fémfeldolgozó Zrt. 4 Ffdm Tivoly 4 Finndent Oy 4 Merge Healthcare Incorporated 4 Atlas Medical Gmb H 3 Bmb Medical 3 Good Medica Spółka Z Ograniczoną Odpowiedzialnością 3 Meril Life Sciences Pvt. Ltd. 3 Ast Vision Care Inc. 2 Aysam Ortopedi Ve Tıbbi Aletler Sanayi Ve Ticaret Limited şirketi 2 Beijing Wandong Medical Technology Co., Ltd. 2 E Pflex Feinwerktechnik Gmb H 2 Lifetech Scientific (Shenzhen) Co., Ltd. 2 M.I.Tech Co., Ltd 2 Med Fibers, Inc. 2 Maccura Biotechnology Co., Ltd. 2 Orbus Neich Medical (Shenzhen) Co.,Ltd 2 Shenzhen Mindray Bio Medical Electronics Co., Ltd. 2 Achim Ruthner Gmb H 1 + More Manufacturers

Competent Authority

Ministry Of Health, Welfare And Sports 44 Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 13 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 8 Finnish Medicines Agency, Supervision And Licences, Medical Device Unit 7 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 7 Turkish Medicine And Medical Devices Agency 7 Federal Agency For Medicines And Health Products / / Health Products Division 6 Nemzeti Népegészségügyi és Gyógyszerészeti Központ 5 De/Ca76 Landesamt Für Arbeitsschutz, Verbraucherschutz Und Gesundheit Abt. Gesundheit Dezernat G4 4 Health Products Regulatory Authority, Medical Devices Department 4 Swedish Medical Products Agency 4 The Office For Registration Of Medicinal Products, Medical Devices And Biocidal Products 4 Agencia Española De Medicamentos Y Productos Sanitarios 3 De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 3 De/Ca29 Regierungspräsidium Darmstadt Abteilung Arbeitsschutz Und Umwelt 3 Austrian National Public Health Institute 2 De/Ca09 Staatliches Gewerbeaufsichtsamt Hannover 2 De/Ca40 Regierungspräsidium Tübingen Referat 25 Sachgebiet Medizinprodukte 2 State Agency Of Medicines, Department Of Medical Devices 2 De/Ca22 Bezirksregierung Münster 1 + More Competent Authorities

Kind

Single Use 23 Sterilization 16 Active 13 Sterile 13 Implantable 4 Measuring Function 3 Professional Testing 3 Reagent 3 Reusable 3 Software 3 Administering Medicine 2 Animal Tissues 2 Kit 2 Instrument 1 Latex 1 Medicinal Product 1 Microbial Substances 1 Orthopedic 1 + More Kinds

Classification

FDA Class 2 45 Eu Md Class 2a 44 Eu Md Class 1 35 Eu Md Class 2b 29 FDA Class 3 24 FDA Class 1 13 Eu Ivd Class A 6 Eu Ivd General 5 Eu Md Class 3 4 FDA Unclassified 2 Eu Ivd Class C 1 FDA Not Classified 1 + More Classifications

Notified Body

Sgs Belgium Nv 29 Bsi Group The Netherlands B.V. 7 Tüv Rheinland Lga Products Gmb H 6 Tüv Süd Product Service Gmb H 4 Dekra Certification B.V. 3 Dqs Medizinprodukte Gmb H 3 Dnv Product Assurance As 2 Eurofins Electric & Electronics Finland Oy 2 Gmed Sas 2 Ht Cert (Health Technology Certification Ltd) 2 Turkish Standards Institution (Tse) 2 Bureau Veritas Italia S.P.A. 1 Dnv Medcert Gmb H 1 Imq Istituto Italiano Del Marchio Di Qualità S.P.A. 1 Intertek Semko Ab 1 Kiwa Cermet Italia S.P.A. 1 Kiwa Belgelendirme Hizmetleri A.ş. 1 Slovenian Institute Of Quality And Metrology Siq 1 Szutest Uygunluk Değerlendirme A.ş. 1 + More Notified Bodies

FDA FEI Number

1000306617 19 2024800 19 3005670738 19 3006330030 19 3001236277 16 1000306431 15 1043214 15 1820334 15 3016678045 15 1000112877 14 1000112968 14 1000219637 14 2124215 14 3005011024 14 3012494290 14 1000138054 13 1000512168 13 2020550 13 2183744 13 3010934856 13 + More FDA FEI Numbers

Regulation

Us FDA 6k Eu Mdd 69 Eu Mdr 43 Eu Ivdr 7 Eu Ivdd 5 + More Regulations

Authorized Representative

Emergo Europe B.V. 31 Med Envoy Global Bv 25 Shanghai International Holding Corp. Gmb H(europe) 10 Obelis S.A. 6 Mdss Gmb H 4 Cmc Medical Devices & Drugs Sl 3 Ar Experts B.V. 2 Bricon Gmb H 2 Certification Experts 2 Humiss International B.V. 2 Inion Oy 2 Ktr Europe Gmb H 2 Life Tech Scientific (Europe) B.V. 2 Prolinx Gmb H 2 Quality First International Oü 2 Sungo Europe B.V. 2 Total Laser Solution Gmb H 2 Young Microbrush Ireland Ltd 2 Mps Medical Product Service Gmb H 1 Acorn Regulatory Consultancy Services Ltd 1 + More Authorized Representatives

FDA Registration Number

2024800 19 2029372 19 3005360469 19 3006330030 19 1649518 16 1043214 15 1820334 15 2029275 15 3016678045 15 1054241 14 1055236 14 1058584 14 2124215 14 3005011024 14 3012494290 14 1061124 13 1319639 13 2020550 13 2183744 13 3010934856 13 + More FDA Registration Numbers

FDA K Number

K760793 1 K813469 1 K820500 1 K860112 1 K863073 1 K874410 1 K891299 1 K924578 1 K924629 1 K940242 1 + More FDA K Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 59 Mdd Annex Ii Section 4 7 Mdd Annex V 4 Mdd Annex Vi 2 Ivdd Annex Iv (Excluding Sections 4, 6) 1 + More Certificate Types

Status

On The Market 59 No Longer On The Market 4 Not Intended For Eu Market 2 + More Statuses

Oclean AirPump Nozzle(N20, N21)

FDA registration

Shenzhen Yunding Information Technology Co.,Ltd.·1 product·🇨🇳 China

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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

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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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