WATER PIK, INC. - BEUDAMED

BEUDAMED

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501 results · 98ms · Sources: EU EUDAMED, US FDA

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FDA UDI 390 Device 81 FDA registration 18 Basic UDI-DI 8 Authorized representative 2 Importer 1 Manufacturer 1 + More Filters

Country

United States 498 France 1 Netherlands 1 Spain 1 + More Countries

Manufacturer

Water Pik, Inc. 90 Angelus Indústria De Produtos Odontológicos S/A 2 Okamoto Rubber Products Co., Ltd. 2 Musculoskeletal Transplant Foundation 1 3 D Industrial Imaging Co.Ltd 1 7 D Surgical Ulc 1 A&D Company, Limited 1 A M Systems 1 Active Life Scientific, Inc. 1 Acutronic Medical Systems Ag 1 Ag Industries Llc 1 Ai Optics Private Limited 1 Ain Medicare Sdn Bhd 1 Air Water Realize Inc. 1 Amtec Co., Ltd. 1 Ark Diagnostics, Inc. 1 Asahi Intecc Co., Ltd. 1 Astec Co.,Ltd 1 Asti Corporation 1 Ava Sciences Fmtc Llc 1 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 91 Agencia Española De Medicamentos Y Productos Sanitarios 1 Ministry Of Health, Welfare And Sports 1 + More Competent Authorities

Kind

Single Use 79 Sterilization 77 + More Kinds

Classification

Eu Md Class 1 89 + More Classifications

FDA FEI Number

1712259 18 + More FDA FEI Numbers

Regulation

Us FDA 408 Eu Mdr 89 + More Regulations

Authorized Representative

Sofibel 90 + More Authorized Representatives

FDA Registration Number

1712259 18 + More FDA Registration Numbers

Status

On The Market 80 No Longer On The Market 1 + More Statuses

Emergo Europe B.V.

Authorized representative

🇳🇱 Netherlands·900 Manufacturers·22100 Devices

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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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