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AirLife 001902A

by Airlife, Inc.

AirLife 001902A is a Class II device made by Airlife, Inc., listed in FDA GUDID since 31 Jan 2020 (UDI-DI 10190752131064), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10190752131064 UDI-DI Date31 Jan 2020ListedStatusListed 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  • Withdrawn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
AirLife
Generic name
Incentive spirometer
Model / Ref / Catalog
001902A
Primary DI / UDI-DI
10190752131064
FDA product code
BWF
GMDN term
Incentive spirometer
Device class
Class II
Regulation number
868.5690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Incentive spirometer

Similar devices

Other devices filed under FDA product code BWF (Spirometer, Therapeutic (Incentive)).

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)