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Halyard ASAB78-04_0002

by Avid Medical, Inc.

Halyard ASAB78-04_0002 is a Class II device made by Avid Medical, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 10809160542248), 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 Number10809160542248 UDI-DI Date29 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  • Withdrawn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
General surgical procedure kit, medicated
Model / Ref / Catalog
ASAB78-04_0002, ASAB78-04
Primary DI / UDI-DI
10809160542248
FDA product code
LRO
GMDN term
General surgical procedure kit, medicated
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Other devices from Avid Medical, Inc.

See all devices from Avid Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)