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SMITHWICK Carotid Shunt WR1409NRS

by Implantable Devices

Listed FDA GUDID listing, not in commercial distribution

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 Number00858764006215 UDI-DI Date24 Oct 2016ListedStatusListed GUDID: not 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  • Withdrawn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
SMITHWICK Carotid Shunt
Generic Name
Carotid artery shunt
Model / Ref / Catalog
WR1409NRS
Primary DI / UDI-DI
00858764006215
FDA Product Code
DXC
GMDN Term
Carotid artery shunt
Device Class
Class II
Regulation Number
870.4450
GUDID distribution status
Not in Commercial Distribution

Other devices from Implantable Devices

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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