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AirLife™ 003020

by Airlife, Inc.

AirLife™ 003020 is a Class I device made by Airlife, Inc., listed in FDA GUDID since 21 Feb 2025 (UDI-DI 10889483571651), 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 Number10889483571651 UDI-DI Date21 Feb 2025ListedStatusListed 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  • Withdrawn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
Heat/moisture exchanger/microbial medical gas filter
Model / Ref / Catalog
003020
Primary DI / UDI-DI
10889483571651
FDA product code
BYD
GMDN term
Heat/moisture exchanger/microbial medical gas filter
Device class
Class I
Regulation number
868.5375
GUDID distribution status
In Commercial Distribution

Related devices

Category: Heat/moisture exchanger/microbial medical gas filter

Similar devices in this category

Other devices filed under Heat/moisture exchanger/microbial medical gas filter.

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)