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F&P OptiPAP Junior OPTIPAPFUS

by Fisher & Paykel Healthcare, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number09420012479549 UDI-DI Date20 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
F&P OptiPAP Junior
Generic Name
Nasal oxygen cannula, CPAP
Model / Ref / Catalog
OPTIPAPFUS
Primary DI / UDI-DI
09420012479549
FDA Product Code
SGR
GMDN Term
Nasal oxygen cannula, CPAP
Device Class
Class II
Regulation Number
868.5895
GUDID distribution status
In Commercial Distribution

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Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No