Consulting Wallah › Device Explorer › Other devices › Carotid artery shunt
Device Explorer · FDA GUDID · GMDN 47113

Carotid artery shunt

A sterile device designed to serve as a temporary blood conduit (a shunt) connecting the distal internal carotid artery to the proximal common carotid artery allowing intravascular blood to continuously flow to the patient's brain during an endarterectomy proc

US‑registered devices90in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
ShareLinkedIn

Share of device records

Lucas Medical Inc5258%
Lemaitre Vascular, Inc.1921%
Integra Lifesciences Corporation1820%
Cardinal Health 200, Llc11%

Top labelers

CompanyDevicesShare
Lucas Medical Inc5258%
Lemaitre Vascular, Inc.1921%
Integra Lifesciences Corporation1820%
Cardinal Health 200, Llc11%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LMI CAROTID ENDARECTOMY SHUNT CATHETERFlexcel Carotid ShuntPruitt F3 Carotid ShuntLMI CAROTID ENDARTERECTOMY SHUNT CATHETERCAROTID ENDARTERECTOMY SHUNTLMI CAROTID SHUNT WITH SAFETY BALLOON CATHETERIntegra®Sundt™MoniTorr™ ICPArgyle

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
MJNCatheter, Intravascular Occluding, Temporary71
DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA42
DXCClamp, Vascular23
DWFCatheter, cannula and tubing, vascular, cardiopulmonary bypa1

GMDN & GCC registration

  • GMDN code 47113 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 22

Use these as the dimensions to specify in a tender line.

No closely related category with 50+ devices.

How many carotid artery shunt products are registered in the US?

90 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Carotid artery shunt", from 4 companies. The largest labeler is Lucas Medical Inc with 58% of records.

Which FDA product codes apply?

MJN (Catheter, Intravascular Occluding, Temporary), DWF (CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA), DXC (Clamp, Vascular), DWF (Catheter, cannula and tubing, vascular, cardiopulmonary bypa)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

Add carotid artery shunt to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Carotid artery shunt

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying carotid artery shunt for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

Get quotes →