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AirLife™ 377PWR90

by Airlife, 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 Number10889483648162 UDI-DI Date14 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  • Withdrawn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
AirLife™
Generic name
Heated respiratory humidifier
Model / Ref / Catalog
377PWR90
Primary DI / UDI-DI
10889483648162
FDA product code
BTT
GMDN term
Heated respiratory humidifier
Device class
Class II
Regulation number
868.5450
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

  • Lot / batch number

Other properties (14)

  • 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
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No