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Halyard ABCP1004

by Owens & Minor Distribution, Inc.

Halyard ABCP1004 is a Class II device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 27 Oct 2026 (UDI-DI 10885632520358), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885632520358 UDI-DI Date27 Oct 2026ListedStatusListed 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  • Withdrawn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
Halyard
Generic name
Anaesthesia breathing circuit, single-use
Model / reference
ABCP1004
Primary DI / UDI-DI
10885632520358
FDA product code
CAH
GMDN term
Anaesthesia breathing circuit, single-use
Device class
Class II
Regulation number
868.5260
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CAH (Filter, bacterial, breathing-circuit).

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

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