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GORE® TAG® Thoracic Branch Endoprosthesis TAC124510A

by W. L. Gore & Associates, 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 Number00733132667024 UDI-DI Date26 May 2026ListedStatusListed 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  • Withdrawn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
GORE® TAG® Thoracic Branch Endoprosthesis
Generic Name
Aortic arch endovascular stent-graft
Model / Ref / Catalog
TAC124510A
Primary DI / UDI-DI
00733132667024
FDA Product Code
MIH
GMDN Term
Aortic arch endovascular stent-graft
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Other devices from W. L. Gore & Associates, Inc.

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No