Skip to content

Halyard VHWV008-08_0001

by Avid Medical, Inc.

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 Number10809160388839 UDI-DI Date4 Nov 2022ListedStatusListed 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  • Withdrawn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
Halyard
Generic Name
Peripheral anaesthesia single-administration set, non-medicated
Model / Ref / Catalog
VHWV008-08_0001, VHWV008-08
Primary DI / UDI-DI
10809160388839
FDA Product Code
OGD
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated
Device Class
Class II
Regulation Number
868.5120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral anaesthesia single-administration set, non-medicated

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