Identity
- Trade Name
- AIRSENSE 10 AUTOSET FH FR EUDAMED
- Device Name
- AirSense 10 AutoSet , AirSense 10 Elite , AirSense 10 AutoSet For Her , AirSense 10 AutoSet No CAM (C2C) EUDAMED
- Model / Reference
- 37422 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00619498374229 EUDAMED
- Basic UDI-DI
- 619498EC1496T EUDAMED
- Direct Marketing DI
- 00619498371303 EUDAMED
- EMDN Code
- Z12030102 CONTINUOUS POSITIVE PRESSURE EQUIPMENT 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
Yes
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
Airsense 10 Autoset Fh Fr 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 | 619498EC1496T | 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 a04f6339-66d4-4046-84fa-107ca5aa45ee 61 fields · synced Jun 18, 2026