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Device Explorer · FDA GUDID · GMDN 47111

Surgical intravascular shunt

A sterile device designed to temporarily channel (shunt) intravascular blood through a vascular anastomosis, primarily to control bleeding and enable distal perfusion during coronary or peripheral vascular bypass grafting and vessel repair surgery. It is typic

US‑registered devices62in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription34%Rx‑only share
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Share of device records

Kdl Medical, Inc.2337%
Medtronic, Inc.1829%
Maquet Cardiovascular Llc1219%
Synovis Life Technologies, Inc.915%

Top labelers

CompanyDevicesShare
Kdl Medical, Inc.2337%
Medtronic, Inc.1829%
Maquet Cardiovascular Llc1219%
Synovis Life Technologies, Inc.915%

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

Brand names on the register (sample)

Sof-Flo Atraumatic Coronary Artery ShuntBulb Tip Coronary Artery ShuntsClearView™Axius Coronary ShuntFlo-Thru Intraluminal Shunt®CLEARVIEW®

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

FDA product codes

CodeNameDevices
DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa23
DWFCatheter, cannula and tubing, vascular, cardiopulmonary bypa16
DXCClamp, Vascular12
DXCCLAMP, VASCULAR9
DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA1
JOLCATHETER AND TIP, SUCTION1

GMDN & GCC registration

  • GMDN code 47111 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 34% · 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

Outer Diameter (Millimeter) · 20Length (Millimeter) · 1

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

No closely related category with 50+ devices.

How many surgical intravascular shunt products are registered in the US?

62 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical intravascular shunt", from 4 companies. The largest labeler is Kdl Medical, Inc. with 37% of records.

Which FDA product codes apply?

DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa), DWF (Catheter, cannula and tubing, vascular, cardiopulmonary bypa), DXC (Clamp, Vascular), DXC (CLAMP, VASCULAR)

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?

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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.

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