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VALIANT® Captivia VAMF4238C150TU

by Medtronic, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169400184 UDI-DIDate23 Sep 2014ListedStatusListed 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  • Withdrawn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
VALIANT® Captivia
Generic Name
Descending thoracic aorta/aortic isthmus endovascular stent-graft
Model / Reference
VAMF4238C150TU
Primary DI / UDI-DI
00643169400184
PMA Number
FDA Product Code
MIH
GMDN Term
Descending thoracic aorta/aortic isthmus endovascular stent-graft
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Descending thoracic aorta endovascular stent-graft

Cleared under the same submission (P100040)

Show all (12)

Similar devices

Also classified as Descending thoracic aorta endovascular stent-graft.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number

Other properties (9)

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