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Inspire IHC607

by Inspiration Healthcare, Ltd.

Inspire IHC607 is a Class I device made by Inspiration Healthcare, Ltd., listed in FDA GUDID since 7 Nov 2016 (UDI-DI 05060206920125), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060206920125 UDI-DI Date7 Nov 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Inspire
Generic name
Nasal oxygen cannula, CPAP
Model / reference
IHC607
Primary DI / UDI-DI
05060206920125
FDA product code
CAT
GMDN term
Nasal oxygen cannula, CPAP
Device class
Class I
Regulation number
868.5340
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nasal oxygen cannula, CPAP

Similar devices in this category

Other devices filed under Nasal oxygen cannula, CPAP.

Other devices from Inspiration Healthcare, Ltd.

See all devices from Inspiration Healthcare, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)