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Vital Signs™ AFPXOXXX

by Airlife, Inc. 2 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10889483595299 UDI-DI Date14 Feb 2025ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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
AFPXOXXX
Primary DI / UDI-DI
10889483595299
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

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
  • Serial Number
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No