Pie Medical Imaging B.V. - BEUDAMED

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122 results · 145ms · Sources: EU EUDAMED, US FDA

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FDA UDI 42 Basic UDI-DI 23 Device 23 FDA 510(k) 22 FDA registration 10 Certificate 1 Manufacturer 1 + More Filters

Country

Netherlands 78 United States 44 + More Countries

Manufacturer

Pie Medical Imaging B.V. 47 + More Manufacturers

Competent Authority

Ministry Of Health, Welfare And Sports 48 + More Competent Authorities

Kind

Active 23 Measuring Function 23 Software 23 + More Kinds

Classification

Eu Md Class 2a 46 FDA Class 2 22 + More Classifications

Notified Body

Tüv Süd Product Service Gmb H 48 + More Notified Bodies

FDA FEI Number

3003595527 31 3000126629 21 3000976525 21 3002807880 21 3004977335 21 3005877899 21 3009077524 21 3009617712 21 1000284313 20 1220246 20 2936485 20 3001675293 20 3002175190 20 3002579136 20 3002808139 20 3002808382 20 3003202425 20 3003481798 20 3006990600 20 3008496839 20 + More FDA FEI Numbers

Regulation

Us FDA 74 Eu Mdd 46 + More Regulations

FDA Registration Number

9710122 31 3000126629 21 3000976525 21 3003768277 21 3004977335 21 3005877899 21 3009077524 21 3009617712 21 1220246 20 2936485 20 3001675293 20 3002579136 20 3003202425 20 3006990600 20 3008496839 20 3010331645 20 3010398867 20 3012075008 20 3012345110 20 3013283620 20 + More FDA Registration Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 48 + More Certificate Types

Status

On The Market 23 + More Statuses

CAAS MRV

FDA Class 2 ·Radiology

CAAS Workstation

FDA Class 2 ·Radiology

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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

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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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