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Vital Signs™ A565192X

by Airlife, Inc.

Vital Signs™ A565192X is a Class I device made by Airlife, Inc., listed in FDA GUDID since 20 Feb 2020 (UDI-DI 10190752120495), 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 Number10190752120495 UDI-DI Date20 Feb 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  • Withdrawn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
Vital Signs™
Generic name
Anaesthesia breathing circuit, single-use
Model / Ref / Catalog
A565192X
Primary DI / UDI-DI
10190752120495
FDA product code
CAI
GMDN term
Anaesthesia breathing circuit, single-use
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution
Size
Length — 60 Inch

Related devices

Category: Anaesthesia breathing circuit, single-use

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

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