Identity
- Trade Name
- AIRTOUCH F20 SML SYS - EU EUDAMED
- Device Name
- AirTouch F20 and AirTouch F20 For Her,AirFit F20 Quiet and AirFit F20 For Her Quiet,AirFit F20 and AirFit F20 For Her,AirFit F20 Non Magnetic EUDAMED
- Model / Reference
- 63034 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00619498630349 EUDAMED
- Basic UDI-DI
- 619498EC1726N EUDAMED
- Direct Marketing DI
- 00619498004102 EUDAMED
- EMDN Code
- R0301010201 CPAP MASKS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Airtouch F20 Sml Sys - Eu by Resmed Pty Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 619498EC1726N | Class IIa | Active |
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Manufacturer
- Manufacturer
- ResMed PTY LTD
- EUDAMED SRN
- AU-MF-000011753
- Authorised Representative
- ResMed SAS FR-AR-000007151
Sources (1)
- EUDAMED fd00572d-b350-45f1-9260-d17e2942bdac 61 fields · synced Jun 18, 2026