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BEUDAMED

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8,881 results · 39ms · Sources: EU EUDAMED, US FDA

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FDA UDI 7k FDA registration 465 Device 410 Basic UDI-DI 407 FDA Pre-Market Approval 274 FDA 510(k) 40 Certificate 7 FDA classification 5 Manufacturer 4 Authorized representative 3 Importer 1 + More Filters

Country

United States 8k China 839 Pakistan 101 United Arab Emirates 60 Germany 59 Bulgaria 26 Hong Kong 21 India 13 Spain 10 United Kingdom 9 Bangladesh 8 France 8 Canada 4 Denmark 4 Malaysia 4 Italy 3 Japan 3 Netherlands 3 South Korea 3 Switzerland 3 + More Countries

Manufacturer

Chongqing Fws Medical Device Co.,Ltd 807 Industrias Hidráulicas Pardo Sl 8 Atmos Medizin Technik Gmb H & Co. Kg 2 New Idem Srl 2 Wenzhou Naisi Health Product Co., Ltd. 2 Alamin For Modern Industries 1 Cixi Bld Medical Instrument Co., Ltd. 1 Jilin Fulanns Medical Technology Co.,Ltd 1 Xiaotao Dingcheng Non Woven Products Co., Ltd 1 2 L Bio Co., Ltd. 1 A & J Dental Products International 1 A1 Globe Sdn. Bhd. 1 Aamedix Glove Sdn Bhd 1 Abi Enterprises 1 Acer Dentallab Co., Limited 1 Acme Tooling Technology Co., Ltd. 1 Acmedi Korea Co.,Ltd. 1 Ads Dental Lab Ltd. 1 Agnitio Science &Technology,Inc. 1 Aie Tech Co., Ltd. 1 + More Manufacturers

Competent Authority

Ministry Of Health, Welfare And Sports 813 Agencia Española De Medicamentos Y Productos Sanitarios 11 De/Ca39, Regierungspräsidium Freiburg Referat 25 2 Federal Agency For Medicines And Health Products / / Health Products Division 2 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 2 De/Ca21 Bezirksregierung Köln Dezernat 24 1 De/Ca304 Marktüberwachung Medizinprodukte Bayern 1 + More Competent Authorities

Kind

Implantable 400 Orthopedic 400 Single Use 400 Sterile 400 Active 2 Kit 2 Professional Testing 2 Reagent 2 Animal Tissues 1 Reprocessed 1 + More Kinds

Classification

Eu Md Class 2b 588 FDA Class 3 273 Eu Md Class 2a 215 FDA Class 1 27 FDA Class 2 18 Eu Md Class 1 12 Eu Ivd General 2 + More Classifications

Notified Body

Udem Uluslararasi Belgelendirme Denetim Egitim Merkezi San. Ve Tic. A.ş. 808 Sgs Belgium Nv 1 Tüv Süd Product Service Gmb H 1 + More Notified Bodies

FDA FEI Number

1920664 259 2936921 259 3001362763 259 3002483854 259 3002807715 259 3003288808 259 3003691824 259 3006695864 259 3012236936 259 3011499367 65 3014233026 56 3018094310 30 3035374386 26 3004216008 23 3005747797 22 3013557562 21 3016965929 21 1417592 20 3010041511 20 3012494290 19 + More FDA FEI Numbers

Regulation

Us FDA 8k Eu Mdd 802 Eu Mdr 13 Eu Ivdd 2 + More Regulations

Authorized Representative

Kingsmead Service B.V. 808 Cmc Medical Devices & Drugs Sl 2 Lotus Nl B.V. 2 Emergo Europe B.V. 1 Greatcare Medical Gmb H 1 Med Path Gmb H 1 Shanghai International Holding Corp. Gmb H(europe) 1 Tokai Optecs Nv 1 + More Authorized Representatives

FDA Registration Number

1920664 259 2936921 259 3002807715 259 3003288808 259 3006695864 259 3007606649 259 3012236936 259 8030392 259 9615030 259 9710340 259 3011499367 65 3014233026 56 3018094310 30 3035374386 26 8040278 23 3011137372 22 1417592 21 3013557562 21 3016965929 21 3010041511 20 + More FDA Registration Numbers

FDA K Number

K032403 1 K061256 1 K801050 1 K803178 1 K831119 1 K831367 1 K842701 1 K853261 1 K854888 1 K854899 1 K871925 1 K875292 1 K890366 1 K891334 1 K891888 1 K892521 1 K902000 1 K930118 1 K932493 1 K935146 1 + More FDA K Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 808 Mdd Annex V 2 + More Certificate Types

Status

On The Market 410 + More Statuses

CMC Medical Devices & Drugs SL

Authorized representative

🇪🇸 Spain·698 Manufacturers·11260 Devices

<1 …441 442 443 444 445 >

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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