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Sign in to claim this brandResmed Corp
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 9001 Spectrum Center Boulevard, San Diego, CA, 92123
- Website
- resmed.com
- —
- —
- [email protected]
- Phone
- 800-424-0737
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000115734
- DUNS Number
- 080243150
Catalogue (404)
Page 5 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Quattro Fx | 61715 | FDA UDI | Class II | Active |
| Mirage Fx | 62118 | FDA UDI | Class II | Active |
| AIRFIT N30i | 63896 | FDA UDI | Class II | Active |
| Nv Quattro Air | 62780 | FDA UDI | Class I | Active |
| AIRFIT N30i | 63805 | FDA UDI | Class II | Active |
| Airfit F 10 | 63229 | FDA UDI | Class II | Active |
| Airfit F30i | 63366 | FDA UDI | Class II | Active |
| Quattro Fx | 61734 | FDA UDI | Class II | Active |
| VPAP Tx | 36048 | FDA UDI | Class II | Active |
| S9 | 36940 | FDA UDI | Class II | Active |
| H4i | 26954 | FDA UDI | Class II | Active |
| RMDpulse | 22254 | FDA UDI | Class II | Active |
| Mirage Liberty | 61348 | FDA UDI | Class II | Active |
| Airfit F40 | 64603 | FDA UDI | Class II | Active |
| Mirage Liberty | 61333 | FDA UDI | Class II | Active |
| Quattro Air | 16127 | FDA UDI | Class II | Active |
| AirTouch F20 | 63002 | FDA UDI | Class II | Active |
| Um/Umii | 16570 | FDA UDI | Class II | Active |
| Mirage Liberty | 61323 | FDA UDI | Class II | Active |
| Swift Fx | 61513 | FDA UDI | Class II | Active |
| RMDpulse | 22253 | FDA UDI | Class II | Active |
| Airfit F20 | 63445 | FDA UDI | Class II | Active |
| Swift Fx Nano | 62263 | FDA UDI | Class II | Active |
| H3i | 33926 | FDA UDI | Class II | Active |
| Mirage Micro | 16379 | FDA UDI | Class II | Active |
| AIRFIT N30i | 63844 | FDA UDI | Class II | Active |
| Ultra Mirage Ffm | 60666 | FDA UDI | Class II | Active |
| ClimateLine Air NA | 37298 | FDA UDI | Class II | Active |
| Mirage Softgel | 61603 | FDA UDI | Class II | Active |
| Sideport | 14915 | FDA UDI | Class II | Unknown |
| AirFit N30 | 64230 | FDA UDI | Class II | Active |
| Mirage Swift | 60530 | FDA UDI | Class II | Active |
| Quattro Fx | 61733 | FDA UDI | Class II | Active |
| Airfit F40 | 64604 | FDA UDI | Class II | Active |
| AirTouch F20 | 63015 | FDA UDI | Class II | Active |
| HumidX Plus | 38811 | FDA UDI | Class I | Active |
| AIRFIT N30i | 63847 | FDA UDI | Class II | Active |
| AirTouch F20 | 63023 | FDA UDI | Class II | Active |
| AIRFIT N30i | 63814 | FDA UDI | Class II | Active |
| AirTouch F20 | 63000 | FDA UDI | Class II | Active |
| Airfit N20 | 63556 | FDA UDI | Class II | Active |
| Airfit F10 | 63129 | FDA UDI | Class II | Active |
| AcuCare | F1-4 | FDA UDI | Class II | Active |
| Mirage Quattro | 61292 | FDA UDI | Class II | Active |
| Um Ffm | 60628 | FDA UDI | Class II | Active |
| Nv Ultra Mirage | 60403 | FDA UDI | Class I | Active |
| Airfit F20 | 63402 | FDA UDI | Class II | Active |
| Quattro Air | 62740 | FDA UDI | Class II | Active |
| AcuCare | F1-1 | FDA UDI | Class II | Active |
| Airfit F30i | 63305 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jul 12, 2016 | Z-2550-2016 | — | terminated | Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask. |
| Jan 13, 2016 | Z-0746-2016 | — | terminated | Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue. |
| Apr 23, 2007 | Z-1006-2007 | — | terminated | S8 devices manufactured between July 2004 and May 15, 2006 are susceptible to fatigue in the connection of the AC appliance inlet connector and the power supply (power cord) leading to possible failure (short circuit, electrical failure, sparks, smoke). |