EUDAMED device
AIRTOUCH F20 LGE SYS - EU
EUDAMED device 00619498630363 · ResMed PTY LTD
Key facts
| Primary DI | 00619498630363 |
|---|---|
| Trade name | AIRTOUCH F20 LGE SYS - EU |
| 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 |
| Reference or catalog number | 63036 |
| Manufacturer | ResMed PTY LTD |
| Manufacturer SRN | AU-MF-000011753 |
| Risk class | Class IIa |
| EMDN code | R0301010201 |
| EMDN description | CPAP MASKS |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Feb 4, 2026 |
At a glance
- No Matching FDA GUDID record
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About EUDAMED devices
EUDAMED is the European Union's database of medical devices registered under the MDR and IVDR, including UDI-DIs, risk classes and EMDN nomenclature codes.
Source: European Commission, European Database on Medical Devices (EUDAMED) · Source date: