Consulting Wallah › Device Explorer › Other devices › Arteriovenous shunt
Device Explorer · FDA GUDID · GMDN 13586

Arteriovenous shunt

An implanted device designed to provide a passage for blood to flow between an artery typically located in an arm, and a peripheral vein, central vein or right atrium, creating a graft fistula that provides blood access for external procedures, especially haem

US‑registered devices58in commercial distribution
Companies3labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription62%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Merit Medical Systems, Inc.2848%
Lemaitre Vascular, Inc.2238%
Thoratec Corporation814%

Top labelers

CompanyDevicesShare
Merit Medical Systems, Inc.2848%
Lemaitre Vascular, Inc.2238%
Thoratec Corporation814%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

HeRO®ProCol Biologic Vascular GraftVECTRA®, VASCULAR ACCESS GRAFTArtegraft Vascular Graft

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

FDA product codes

CodeNameDevices
DSYPROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER27
LXATissue Graft Of 6mm And Greater26
DSYProsthesis, Vascular Graft, Of 6mm And Greater Diameter9
MSDCatheter, Hemodialysis, Implanted9
LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than4
LJSCatheter,Intravascular,Therapeutic,Long-Term Greater Than 304

GMDN & GCC registration

  • GMDN code 13586 · implantable
  • Single‑use 100% · sterile 100% · Rx‑only 62% · 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

Lumen/Inner Diameter (Millimeter) · 6Length (Centimeter) · 6Outer Diameter (Millimeter) · 1

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

No closely related category with 50+ devices.

How many arteriovenous shunt products are registered in the US?

58 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arteriovenous shunt", from 3 companies. The largest labeler is Merit Medical Systems, Inc. with 48% of records.

Which FDA product codes apply?

DSY (PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER), LXA (Tissue Graft Of 6mm And Greater), DSY (Prosthesis, Vascular Graft, Of 6mm And Greater Diameter), MSD (Catheter, Hemodialysis, Implanted)

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.

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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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