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myAirvo 3 900PT470

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 9 Nov 2026. What this means

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number09420012466426 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
myAirvo 3
Generic name
Digital storage media
Model / Ref / Catalog
900PT470
Primary DI / UDI-DI
09420012466426
FDA product code
OUG
GMDN term
Digital storage media
Device class
Class I
Regulation number
880.6310
GUDID distribution status
In Commercial Distribution

Other devices from Fisher & Paykel Healthcare, Inc.

See all devices from Fisher & Paykel Healthcare, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No