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3,541 results · 37ms · Sources: EU EUDAMED, US FDA

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FDA UDI 2k FDA registration 1k FDA 510(k) 278 Device 30 Basic UDI-DI 21 Manufacturer 5 FDA classification 4 Authorized representative 2 Importer 2 FDA Pre-Market Approval 1 + More Filters

Country

United States 3k India 283 China 123 Germany 42 South Korea 36 Pakistan 31 Finland 30 Malaysia 26 United Kingdom 24 Netherlands 18 Canada 15 Mexico 15 Vietnam 14 Japan 7 Hungary 6 Italy 5 Hong Kong 4 Taiwan 3 Austria 2 Cambodia 2 + More Countries

Manufacturer

Sairex Ky 20 Shenzhen Keborui Electronics Co., Ltd 14 A&D Company, Limited 5 Suomen Laitostekstiilit Ky 4 Acomed Industrial Co., Ltd. 2 Aero Pro Co., Ltd. 2 Anhui Jucheng Plastic Technology Co., Ltd. 2 Aplan Well Enterprise Co., Ltd. 2 Babylove Industrial Co., Ltd. 2 Bestcare Medical Co., Ltd. 2 Better Enterprise Co., Ltd. 2 Bihua Industry Corp. 2 Biofast Biotech Originality Study Co., Ltd. 2 Bliss Health Products Co., Ltd. 2 Charming World Inc. 2 Combo (Zhongshan) Medical Equipment Co., Ltd. 2 Comfort Orthopedic Co., Ltd. 2 Comfort Plus Corporation 2 Dentmate Technology 2 Daily Life Medical Inc. 2 + More Manufacturers

Competent Authority

Finnish Medicines Agency, Supervision And Licences, Medical Device Unit 30 De/Ca82, Landesdirektion Sachsen Referat Marktüberwachung 14 Ministry Of Health, Welfare And Sports 6 De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 3 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 2 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 2 Agencia Española De Medicamentos Y Productos Sanitarios 1 De/Ca37, Regierungspräsidium Stuttgart 1 De/Ca38 Regierungspräsidium Karlsruhe 1 + More Competent Authorities

Kind

Reprocessed 4 Single Use 4 Animal Tissues 1 Kit 1 Professional Testing 1 Reagent 1 Sterile 1 Sterilization 1 + More Kinds

Classification

FDA Class 2 189 FDA Class 1 77 Eu Md Class 1 47 FDA Unclassified 13 Eu Ivd Class B 2 Eu Ivd Class A 1 Eu Md Class 2a 1 FDA Class 3 1 + More Classifications

Notified Body

Dnv Medcert Gmb H 1 + More Notified Bodies

FDA FEI Number

3013846070 190 3012421607 123 3013718871 86 1220477 85 1417592 85 3006759904 84 3012494290 84 3013557562 84 3001236905 80 1928237 72 1043214 69 3005747797 65 1000306431 64 3001236277 61 3026408938 61 3018094310 60 2110898 58 1000112877 57 3002750084 57 1000112968 56 + More FDA FEI Numbers

Regulation

Us FDA 3k Eu Mdr 47 Eu Ivdr 3 Eu Mdd 1 + More Regulations

Authorized Representative

Tri Rad Medical Gmb H 14 Emergo Europe B.V. 5 Shanghai International Holding Corp. Gmb H(europe) 2 Komas Medical Technology Gmb H 1 Y. Sung Handelsvertretung 1 + More Authorized Representatives

FDA Registration Number

3013846070 190 3012421607 123 3013718871 86 1220477 85 1417592 85 3009171251 84 3012494290 84 3013557562 84 1423537 81 1928237 73 1043214 69 3011137372 65 2029275 63 1649518 61 3026408938 61 3018094310 60 1836161 58 2110898 58 1054241 57 1055236 56 + More FDA Registration Numbers

FDA K Number

K032408 1 K032625 1 K050730 1 K051953 1 K052370 1 K052477 1 K052714 1 K053055 1 K061042 1 K071055 1 K081143 1 K082207 1 K092030 1 K101676 1 K110796 1 K121524 1 K123118 1 K123416 1 K140807 1 K150702 1 + More FDA K Numbers

Certificate Type

Mdd Annex V 1 + More Certificate Types

Status

On The Market 30 + More Statuses

Y. Sung Handelsvertretung

Authorized representative

🇩🇪 Germany·80 Manufacturers

<1 …174 175 176 177 178 >

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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