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Relay Plus Thoracic Stent-Graft System 28-M336250322490U

by Bolton Medical Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00843576102408 UDI-DI Date2 Feb 2021ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Relay Plus Thoracic Stent-Graft System
Generic Name
Descending thoracic aorta/aortic isthmus endovascular stent-graft
Model / Ref / Catalog
28-M336250322490U
Primary DI / UDI-DI
00843576102408
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
Size
Catheter Gauge — 24 French
Outer Diameter — 36 Millimeter
Length — 250 Millimeter
Outer Diameter — 32 Millimeter

Related devices

Category: Descending thoracic aorta endovascular stent-graft

Cleared under the same submission (P110038)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch 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
  • Serial Number: No