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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 4 of 9

Device	Model / Reference	Registries	Class	Status
H4i	24927	FDA UDI	Class II	Active
Swift Lt	60577	FDA UDI	Class II	Active
AirFit P10	62947	FDA UDI	Class II	Active
Remote Alarm	27903	FDA UDI	Class II	Active
S9	36050	FDA UDI	Class II	Active
Resmed	16637	FDA UDI	Class II	Active
Quattro Fx	62501	FDA UDI	Class II	Active
Mirage Softgel	61601	FDA UDI	Class II	Active
AIRFIT N30i	63807	FDA UDI	Class II	Active
Aircurve	37385	FDA UDI	Class II	Active
Airfit F40	64609	FDA UDI	Class II	Active
Mirage Activa Lt	60169	FDA UDI	Class II	Active
Nv Um Ffm	60647	FDA UDI	Class I	Active
Um Ffm	60627	FDA UDI	Class II	Active
Mirage Swift Ii	60540	FDA UDI	Class II	Active
Airfit N 10	63260	FDA UDI	Class II	Active
ResScan	31338	FDA UDI	Class II	Active
myAir	22246	FDA UDI	Class II	Active
AirTouch F20	63016	FDA UDI	Class II	Active
Mirage Activa Lt	60172	FDA UDI	Class II	Active
Airfit N20	63550	FDA UDI	Class II	Active
Mirage Swift	60524	FDA UDI	Class II	Active
AIRFIT N30i	63802	FDA UDI	Class II	Active
HUMIDAIRE 2i	30961	FDA UDI	Class II	Active
Swift Lt	60578	FDA UDI	Class II	Active
Airfit F20	63497	FDA UDI	Class II	Active
ResScan	31334	FDA UDI	Class II	Active
Swift Lt	60595	FDA UDI	Class II	Active
Mirage Softgel	61633	FDA UDI	Class II	Active
Airfit F30i	63369	FDA UDI	Class II	Active
AirFit N20	63504	FDA UDI	Class II	Active
S8	33923	FDA UDI	Class II	Active
AIRFIT N30i	63821	FDA UDI	Class II	Active
Mirage Softgel	61627	FDA UDI	Class II	Active
AcuCare	F1-1	FDA UDI	Class II	Active
AIRFIT P30i	63853	FDA UDI	Class II	Active
AirFit X30i	64350	FDA UDI	Class II	Active
AcuCare	F1-0	FDA UDI	Class I	Active
Airfit F30i	63334	FDA UDI	Class II	Active
HumidX	38808	FDA UDI	Class I	Active
S9	36003	FDA UDI	Class II	Active
Mirage Swift Ii	60537	FDA UDI	Class II	Active
Air 11	39205	FDA UDI	Class II	Active
Swift Lt	60584	FDA UDI	Class II	Active
EasyCare Tx	25944	FDA UDI	Class II	Active
S9	36920	FDA UDI	Class II	Active
Mirage Activa	60122	FDA UDI	Class II	Active
AcuCare	60786	FDA UDI	Class I	Active
Airfit F40	64635	FDA UDI	Class II	Active
Astral	27926	FDA UDI	Class II	Unknown

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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).