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AirLife™ T62

by Airlife, Inc. 2 variants

AirLife™ T62 is a Class I device made by Airlife, Inc., listed in FDA GUDID since 18 Feb 2025 (UDI-DI 10889483606254), 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 Number10889483606254 UDI-DI Date18 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  • Withdrawn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
Airway suction catheter
Model / Ref / Catalog
T62
Primary DI / UDI-DI
10889483606254
FDA product code
BSY
GMDN term
Airway suction catheter
Device class
Class I
Regulation number
868.6810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Airway suction catheter

Similar devices in this category

Other devices filed under Airway suction catheter.

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)