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Resmed Corp

Last updated September 17, 2026

Information

Country: US
Address: 9001 Spectrum Center Boulevard, San Diego, CA, 92123
Website: resmed.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 800-424-0737
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000115734
DUNS Number: 080243150

Catalogue (404)

Page 6 of 9

Device	Model / Reference	Registries	Class	Status
Airtouch N30i	62330	FDA UDI	Class II	Active
Hospital Ffm	60703	FDA UDI	Class II	Active
AirTouch N20	63901	FDA UDI	Class II	Active
Mirage Fx	62136	FDA UDI	Class II	Active
Resmed	16606	FDA UDI	Class II	Active
Pixi	61030	FDA UDI	Class II	Active
Nv Quattro Fx	61742	FDA UDI	Class I	Active
HUMIDAIRE 3i	33947	FDA UDI	Class II	Active
Airfit F20	63401	FDA UDI	Class II	Active
Airsense	37402	FDA UDI	Class II	Active
Air Tubing	14922	FDA UDI	Class I	Active
Mirage Swift	60523	FDA UDI	Class II	Active
myAir	22245	FDA UDI	Class II	Active
AIRFIT N30i	63811	FDA UDI	Class II	Active
Airfit N 10	63230	FDA UDI	Class II	Active
Astral Slimbag Bed Support	27979	FDA UDI	Class II	Active
Airfit F10	63169	FDA UDI	Class II	Active
Headgear	16119	FDA UDI	Class II	Active
Swift Fx Mask Sys-Slm	61508	FDA UDI	Class II	Active
Air 11	39300	FDA UDI	Class II	Active
AIRFIT N30i	63800	FDA UDI	Class II	Active
Mirage Activa Lt	60192	FDA UDI	Class II	Active
S9	36941	FDA UDI	Class II	Active
Swift Fx	61583	FDA UDI	Class II	Active
Mirage Quattro	61290	FDA UDI	Class II	Active
Mirage Activa Lt	60177	FDA UDI	Class II	Active
Mirage Quattro	61265	FDA UDI	Class II	Active
Mirage Fx	62126	FDA UDI	Class II	Active
Airview	22240	FDA UDI	Class II	Active
Quattro Fx	62507	FDA UDI	Class II	Active
H3i	33927	FDA UDI	Class II	Active
Mirage Quattro	61260	FDA UDI	Class II	Active
AcuCare	F1-1	FDA UDI	Class II	Active
Astral Double Limb Adaptor	27980	FDA UDI	Class II	Active
Airfit N20	63542	FDA UDI	Class II	Active
Airfit N20	63507	FDA UDI	Class II	Active
AcuCare	F1-1	FDA UDI	Class II	Active
S9	36850	FDA UDI	Class II	Active
Airfit N20	63505	FDA UDI	Class II	Active
Swift Fx	K090244	FDA 510(k)	Class II	Active
Rescan	K034033	FDA 510(k)	Class II	Active
Autoset Spirit System	K032480	FDA 510(k)	Class II	Active
Geo	K121705	FDA 510(k)	Class II	Active
Vpap Iii St-A	K093731	FDA 510(k)	Class II	Active
Vpap Tx	K092186	FDA 510(k)	Class II	Active
Humidaire 2i	K080797	FDA 510(k)	Class II	Active
Mirage Activa Mask	K032916	FDA 510(k)	Class II	Active
Easycare Tx, Tx Link	K092026	FDA 510(k)	Class II	Active
VPAP Adapt SV, VPAP Tx, S9 VPAP Tx	K161487	FDA 510(k)	Class II	Active
Sullivan Vpap Ii St Nasal Vpap System	K961783	FDA 510(k)	Class II	Active

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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).