EJJ - BEUDAMED

BEUDAMED

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9,662 results · 37ms · Sources: EU EUDAMED, US FDA

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FDA UDI 9k FDA 510(k) 287 FDA registration 93 Device 19 Basic UDI-DI 11 FDA classification 4 Importer 2 Manufacturer 2 Authorized representative 1 + More Filters

Country

United States 10k United Kingdom 21 France 15 Australia 7 Canada 7 Spain 7 India 5 Pakistan 5 China 4 Germany 4 Netherlands 4 South Korea 4 Taiwan 3 Belize 2 Malaysia 2 Colombia 1 Hong Kong 1 Hungary 1 Ireland 1 Israel 1 + More Countries

Manufacturer

Rocamed France 14 Becker Orthopedic Appliance Company 12 General Life Biotechnology Co., Ltd. 1 Patella 96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság 1 Pride Mobility Products Corporation 1 Prosum Medical Limited 1 Shanghai Kindly Enterprise Development Group Co., Ltd. 1 Welt Corp. 1 Zhejiang Kindly Medical Devices Co., Ltd. 1 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 15 Health Products Regulatory Authority, Medical Devices Department 13 Ministry Of Health, Welfare And Sports 3 Malta Medicines Authority 2 De/Ca09 Staatliches Gewerbeaufsichtsamt Hannover 1 Nemzeti Népegészségügyi és Gyógyszerészeti Központ 1 + More Competent Authorities

Kind

Implantable 7 Single Use 7 Sterile 7 Active 1 Instrument 1 Kit 1 Near Patient Testing 1 Professional Testing 1 Self Testing 1 Software 1 + More Kinds

Classification

FDA Class 2 250 FDA Class 1 36 Eu Md Class 1 15 Eu Md Class 2b 14 FDA Unclassified 4 Eu Ivd Annex 2 List B 1 + More Classifications

Notified Body

Gmed Sas 14 Tüv Rheinland Lga Products Gmb H 1 + More Notified Bodies

FDA FEI Number

3013557562 165 3012494290 158 3012421607 137 3006066614 101 3026297922 100 2183301 99 3010862763 96 3004140838 82 2024312 81 2244812 79 3012187973 79 3012627824 78 1316092 77 2515379 77 3009496224 77 2020703 76 3003794907 76 3008912871 76 3009687539 76 4108 75 + More FDA FEI Numbers

Regulation

Us FDA 10k Eu Mdr 15 Eu Mdd 14 Eu Ivdd 1 + More Regulations

Authorized Representative

Acorn Regulatory Consultancy Services Ltd 12 Advena Limited 1 Cmc Medical Devices & Drugs Sl 1 Mdss Gmb H 1 Pride Mobility Products Europe Bv 1 + More Authorized Representatives

FDA Registration Number

3013557562 165 3012494290 158 3012421607 137 3006066614 101 3026297922 100 2183301 99 3010864832 97 3004140838 82 2024312 81 2244812 79 3012187973 79 3012627824 78 1316092 77 2515379 77 3009496224 77 2020703 76 2648744 76 3003794907 76 3008912871 76 8030067 75 + More FDA Registration Numbers

FDA K Number

K002808 1 K002810 1 K002811 1 K011801 1 K013124 1 K020452 1 K031658 1 K032152 1 K033434 1 K051010 1 K053114 1 K760980 1 K771383 1 K771403 1 K780967 1 K780997 1 K781242 1 K790448 1 K790874 1 K801639 1 + More FDA K Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 14 Ivdd Annex Iv (Excluding Sections 4, 6) 1 + More Certificate Types

Status

On The Market 19 + More Statuses

EJ BUSUTTIL LTD

E. J. Bodkin + Co Limited

Authorized representative

🇮🇪 Ireland

<1 …480 481 482 483 484 >

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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