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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 2 of 9

Device	Model / Reference	Registries	Class	Status
Mirage Quattro	61271	FDA UDI	Class II	Active
Hospital Ffm	60704	FDA UDI	Class II	Active
Airfit N 10	63207	FDA UDI	Class II	Active
Mirage Activa Lt	60148	FDA UDI	Class II	Active
Astral	21356	FDA UDI	Class II	Unknown
Quattro Fx	61700	FDA UDI	Class II	Active
Swift Lt	60571	FDA UDI	Class II	Active
AcuCare	F1-0	FDA UDI	Class I	Active
Mirage Swift Ii	60512	FDA UDI	Class II	Active
H4i	26955	FDA UDI	Class II	Active
Airfit F30i	63301	FDA UDI	Class II	Active
Mirage Activa Lt	16387	FDA UDI	Class II	Active
Airtouch N30i	62314	FDA UDI	Class II	Active
H5i	36894	FDA UDI	Class II	Active
Airfit F20	63448	FDA UDI	Class II	Active
Airfit F20	63467	FDA UDI	Class II	Active
Mirage Ffm	16674	FDA UDI	Class II	Active
Resmed	14999	FDA UDI	Class I	Active
Airfit N20	63545	FDA UDI	Class II	Active
Astral 150	27003R	FDA UDI	Class II	Active
Airtouch N30i	62307	FDA UDI	Class II	Active
AcuCare	F1-4	FDA UDI	Class II	Active
Airfit F30i	63351	FDA UDI	Class II	Active
Mirage Activa Lt	60195	FDA UDI	Class II	Active
Mirage Liberty	61301	FDA UDI	Class II	Active
Hypo Filter	21926	FDA UDI	Class II	Active
Resmed	24991	FDA UDI	Class II	Active
S9	36942	FDA UDI	Class II	Active
Mobi Mounting Straps	35055	FDA UDI	Class II	Unknown
Swift Fx Nano	62251	FDA UDI	Class II	Active
Airfit P 10	62900	FDA UDI	Class II	Active
Airfit F40	64602	FDA UDI	Class II	Active
Swift Fx	61575	FDA UDI	Class II	Active
ResScan	31339	FDA UDI	Class II	Active
AIRFIT P30i	63861	FDA UDI	Class II	Active
AirMini	38824	FDA UDI	Class II	Active
AirView	22240	FDA UDI	Class II	Active
Mirage Activa	60101	FDA UDI	Class II	Active
AirFit N30	64219	FDA UDI	Class II	Active
Mirage Liberty	61321	FDA UDI	Class II	Active
Meridian	61103	FDA UDI	Class II	Unknown
Air 11	39301	FDA UDI	Class II	Active
Airfit F20	63469	FDA UDI	Class II	Active
Vpap	26923	FDA UDI	Class II	Active
Homecare	27948	FDA UDI	Class I	Active
Airfit N20	63547	FDA UDI	Class II	Active
AirTouch N20	63903	FDA UDI	Class II	Active
AirFit F20	63475	FDA UDI	Class II	Active
AirFit X30i	64355	FDA UDI	Class II	Active
AirFit N30	64210	FDA UDI	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).