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Veronail Titanium Trochanteric Nail 1

by Orthofix, Inc. 76 variants

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 Number18032937167739 UDI-DI Date16 Sep 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  • Withdrawn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
Veronail Titanium Trochanteric Nail
Generic Name
Orthopaedic guidewire, reusable
Model / Ref / Catalog
1, 17972
Description
CEPHALIC WIRE D. 4MM L 400MM
Primary DI / UDI-DI
18032937167739
FDA Product Code
HSB
GMDN Term
Orthopaedic guidewire, reusable
Device Class
Class II
Regulation Number
888.3020
GUDID distribution status
In Commercial Distribution
Size
Length — 400 Millimeter
Outer Diameter — 4 Millimeter

Related devices

Category: Orthopaedic guidewire, reusable

Other devices from Orthofix, Inc.

See all devices from Orthofix, Inc. →

Properties

  • Sterile
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No