Spident Co., Ltd. - BEUDAMED

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101 results · 103ms · Sources: EU EUDAMED, US FDA

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FDA UDI 51 FDA registration 28 FDA 510(k) 17 Importer 3 Authorized representative 2 + More Filters

Country

United States 53 South Korea 43 France 2 Netherlands 2 Spain 1 + More Countries

Manufacturer

Spident 5 Ampall 2 Angelus Indústria De Produtos Odontológicos S/A 2 C K Dental Ind.Co.,Ltd. 2 Curexo, Inc. 2 Chiaro Technology Limited 2 Clari Pi Inc. 2 Cowellmedi Co., Ltd. 2 Dentalmax Co., Ltd 2 Diadent Group International 2 Dio Corporation 2 Dms Co., Ltd. 2 Dream Con Co., Ltd. 2 E Wha Meditech Inc. 2 Gonimed Co.,Ltd 2 Gyrozen 2 Guilin Woodpecker Medical Instrument Co., Ltd. 2 Hexar Humancare Co.,Ltd 2 Huvexel Co., Ltd. 2 Huanghua Promisee Dental Co.Ltd. 2 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 2 Ministry Of Health, Welfare And Sports 2 Agencia Española De Medicamentos Y Productos Sanitarios 1 + More Competent Authorities

Classification

FDA Class 2 17 + More Classifications

FDA FEI Number

3006113314 45 1718912 17 2024312 17 2411797 17 2515379 17 3002718942 17 3003667632 17 3005628474 17 3006066614 17 3008822460 17 3011689956 17 3012187973 17 3012421607 17 3012494290 17 3026297922 17 3032312561 17 1000231788 16 1215305 16 1281412 16 1410097 16 + More FDA FEI Numbers

Regulation

Us FDA 96 + More Regulations

FDA Registration Number

3006113314 45 1718912 17 2024312 17 2411797 17 2515379 17 3005628474 17 3006066614 17 3008822460 17 3011689956 17 3012187973 17 3012421607 17 3012494290 17 3026297922 17 3032312561 17 8010908 17 9681210 17 1215305 16 1281412 16 1410097 16 1413475 16 + More FDA Registration Numbers

Internacional Ventur S.A.

🇪🇸 Spain·23 Manufacturers

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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