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AirLife™ 205902

by Vyaire Medical, Inc.

AirLife™ 205902 is a Class I device made by Vyaire Medical, Inc., listed in FDA GUDID since 15 Jan 2020 (UDI-DI 10190752131262), 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 Number10190752131262 UDI-DI Date15 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  • Withdrawn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
Breathing circuit catheter mount, single-use
Model / Ref / Catalog
205902
Primary DI / UDI-DI
10190752131262
FDA product code
CAI
GMDN term
Breathing circuit catheter mount, single-use
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Breathing circuit catheter mount, single-use

Similar devices in this category

Other devices filed under Breathing circuit catheter mount, single-use.

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Properties

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