LFK - BEUDAMED

BEUDAMED

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4,361 results · 37ms · Sources: EU EUDAMED, US FDA

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FDA registration 2k Device 994 FDA Pre-Market Approval 873 FDA UDI 533 FDA 510(k) 148 Basic UDI-DI 16 Manufacturer 5 FDA classification 4 Authorized representative 3 Importer 3 System producer 2 Certificate 1 + More Filters

Country

United States 3k South Korea 733 China 272 France 272 Switzerland 110 Sri Lanka 101 Canada 80 Ireland 64 Germany 55 United Kingdom 47 Pakistan 22 Hong Kong 16 Poland 9 Türkiye 7 India 4 Thailand 4 Malaysia 3 Taiwan 3 Israel 2 Italy 2 + More Countries

Manufacturer

Becker Orthopedic Appliance Company 991 Dynamiker Biotechnology (Tianjin) Co., Ltd. 4 İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.ş. 4 Centurion Medical Products, Lp (F/K/A Centurion Medical Products Corporation) 3 Bio Fynder Limited 2 Cook Bio Device 2 Cook Incorporated 2 Molecular Products Ltd 2 Shenzhen Mindray Bio Medical Electronics Co., Ltd. 2 3 A Medical Products Co., Ltd 1 4 L Health Co., Ltd 1 Apt Medical Inc. 1 Ave Science & Technology Co., Ltd. 1 Accucise Diagnostics Inc. 1 Acoresmed Co., Ltd. 1 Acoustic Life Science Co., Ltd. 1 Aikang Med Tech Co., Ltd 1 Aike (Shanghai) Medical Instrument Co., Ltd 1 Allmed Medical Products Co.,Ltd 1 Alton (Shanghai) Medical Instruments Co., Ltd. 1 + More Manufacturers

Competent Authority

Health Products Regulatory Authority, Medical Devices Department 995 Ministry Of Health, Welfare And Sports 9 The Office For Registration Of Medicinal Products, Medical Devices And Biocidal Products 6 Turkish Medicine And Medical Devices Agency 5 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 4 Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 3 Agencia Española De Medicamentos Y Productos Sanitarios 1 De/Ca38 Regierungspräsidium Karlsruhe 1 + More Competent Authorities

Kind

Professional Testing 11 Kit 9 Reagent 9 Animal Tissues 7 Near Patient Testing 3 Single Use 3 Human Tissues 2 Reprocessed 2 Instrument 1 Microbial Substances 1 Self Testing 1 + More Kinds

Classification

Eu Md Class 1 992 FDA Class 3 869 FDA Class 2 123 FDA Class 1 31 Eu Ivd General 7 Eu Md Class 3 4 Eu Md Class 2a 3 FDA Unclassified 2 Eu Ivd Annex 2 List B 1 Eu Ivd Class A 1 Eu Ivd Class B 1 Eu Ivd Class C 1 + More Classifications

Notified Body

Udem Uluslararasi Belgelendirme Denetim Egitim Merkezi San. Ve Tic. A.ş. 4 Polskie Centrum Badan I Certyfikacji S.A. 2 Tüv Süd Product Service Gmb H 1 + More Notified Bodies

FDA FEI Number

2246552 708 1000306216 705 3003120897 705 3004369318 705 3004593495 705 3005700659 705 3018094310 705 1000514656 704 1221541 704 1526611 704 2182207 704 2183319 704 2523676 704 3003166194 704 3003174284 704 3009183442 704 3015537318 704 3030198397 704 1219913 160 2122870 160 + More FDA FEI Numbers

Regulation

Us FDA 3k Eu Mdr 995 Eu Ivdd 8 Eu Mdd 4 Eu Ivdr 3 + More Regulations

Authorized Representative

Acorn Regulatory Consultancy Services Ltd 991 Lotus Nl B.V. 5 Pure Ce B.V. 4 Riomavix Ltd 4 Shanghai International Holding Corp. Gmb H(europe) 3 Medical Device Management Ltd 2 Sungo Europe B.V. 2 Emergo Europe B.V. 1 Obelis S.A. 1 + More Authorized Representatives

FDA Registration Number

2246552 708 1722746 705 2135338 705 3003120897 705 3004209178 705 3004593495 705 3018094310 705 1221541 704 1422634 704 1526611 704 2032227 704 2182207 704 2183319 704 2523676 704 3003174284 704 3009183442 704 3015537318 704 3030198397 704 1219913 160 2122870 160 + More FDA Registration Numbers

FDA K Number

K012571 1 K030598 1 K043225 1 K043315 1 K043358 1 K050343 1 K083060 1 K093702 1 K100537 1 K111794 1 K124033 1 K132566 1 K133672 1 K143562 1 K150524 1 K151405 1 K161693 1 K170456 1 K170955 1 K173627 1 + More FDA K Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 4 Mdd Annex Ii Section 4 4 Mdr Qms 2 Ivdd Annex Iv (Excluding Sections 4, 6) 1 + More Certificate Types

Status

On The Market 994 + More Statuses

Shanghai International Holding Corp. GmbH(Europe)

Authorized representative

🇩🇪 Germany·637 Manufacturers·33064 Devices

<1 …215 216 217 218 219 >

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

BEUDAMED

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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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