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Halyard DUPD23-02_0004

by Avid Medical, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10809160513385 UDI-DIDate20 Feb 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Halyard
Generic Name
General surgical procedure kit, medicated
Model / Ref / Catalog
DUPD23-02_0004, DUPD23-02
Primary DI / UDI-DI
10809160513385
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

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No