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AVID TruCustom VHWV007-06_0009

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 Number10809160117989 UDI-DI Date22 Dec 2016ListedStatusListed 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  • Withdrawn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
AVID TruCustom
Generic Name
Neurosurgical procedure kit, medicated
Model / Ref / Catalog
VHWV007-06_0009, VHWV007-06
Primary DI / UDI-DI
10809160117989
FDA Product Code
OJG
GMDN Term
Neurosurgical procedure kit, medicated
Device Class
Class I
Regulation Number
882.4525
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Related devices

Category: Neurosurgical procedure kit, medicated

Other devices from Avid Medical, Inc.

See all devices from Avid Medical, Inc. →

Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Implantable: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No