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TriVerse X-Ray Digital Template, Tibial 40 MM Keel 02-039-95-3479

by Signature Orthopaedics Pty Ltd

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 Number09348215114374 UDI-DI Date19 Jul 2023ListedStatusListed 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  • Withdrawn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
TriVerse X-Ray Digital Template, Tibial 40 MM Keel
Generic Name
Surgical implant template, reusable
Model / Reference
02-039-95-3479
Primary DI / UDI-DI
09348215114374
FDA Product Code
HWT
GMDN Term
Surgical implant template, reusable
Device Class
Class I
Regulation Number
888.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical implant template, reusable

Other devices from Signature Orthopaedics Pty Ltd

See all devices from Signature Orthopaedics Pty Ltd →

Properties

  • Prescription Use
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No