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BEUDAMED

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21 results · 49ms · Sources: EU EUDAMED, US FDA

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FDA UDI 6 FDA registration 5 FDA 510(k) 4 Device 3 Basic UDI-DI 2 Manufacturer 1 + More Filters

Country

France 14 United States 7 + More Countries

Manufacturer

Gleamer 5 + More Manufacturers

Competent Authority

Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 6 + More Competent Authorities

Kind

Active 2 Software 2 Measuring Function 1 + More Kinds

Classification

Eu Md Class 2a 5 FDA Class 2 4 + More Classifications

FDA FEI Number

3021907554 8 2126677 3 3003377038 3 3014661828 3 3013427569 2 3017840913 2 3019544554 2 3021887566 2 3022719380 2 3026753394 2 3026970882 2 3027453703 2 1000116912 1 1000185293 1 1000284313 1 1000514697 1 1826555 1 2243471 1 2518586 1 2936485 1 + More FDA FEI Numbers

Regulation

Us FDA 15 Eu Mdr 5 + More Regulations

FDA Registration Number

3021907554 8 2126677 3 3014661828 3 9616047 3 3013427569 2 3017840913 2 3019544554 2 3021887566 2 3022719380 2 3026753394 2 3026970882 2 3027453703 2 1226773 1 1423253 1 1644408 1 1651903 1 1826555 1 1836549 1 2032350 1 2243471 1 + More FDA Registration Numbers

Status

On The Market 3 + More Statuses

AIRFIT F30I

RESMED PTY LTD·00619498633340·AIRFIT F30i SYS - M/LGE - AMER

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

BEUDAMED

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API Documentation
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Imprint

BEUDAMED

Rationale
MDR Notified Bodies
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Tools

510(k) Predicate Finder
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510(k) Review Times
21 CFR Regulations
NB Comparison

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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