Consulting Wallah › Device Explorer › Cardiovascular › Central/peripheral venous endovascular stent-graft
Device Explorer · FDA GUDID · GMDN 61856

Central/peripheral venous endovascular stent-graft

A non-bioabsorbable tubular device designed to be implanted in a central and/or peripheral vein (e.g., subclavian, brachiocephalic) to maintain vessel lumen patency, typically to treat stenosis in the outflow of an arteriovenous fistula (AVF) or graft used for

US‑registered devices212in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Angiomed Gmbh & Co. Medizintechnik Kg8540%
Bard Peripheral Vascular, Inc.6832%
Merit Medical Systems, Inc.5225%
Endologix Llc73%

Top labelers

CompanyDevicesShare
Angiomed Gmbh & Co. Medizintechnik Kg8540%
Bard Peripheral Vascular, Inc.6832%
Merit Medical Systems, Inc.5225%
Endologix Llc73%

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

Brand names on the register (sample)

Fluency® Endovascular Stent GraftWRAPSODY®TORUS Stent Graft SystemCOVERA

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

FDA product codes

CodeNameDevices
PFVSystem, endovascular graft, arteriovenous (AV) dialysis acce211
QWMStent Graft, Bypass, Superficial Femoral Artery14

GMDN & GCC registration

  • GMDN code 61856 · 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

No structured size data on the register.

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

How many central/peripheral venous endovascular stent-graft products are registered in the US?

212 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Central/peripheral venous endovascular stent-graft", from 4 companies. The largest labeler is Angiomed Gmbh & Co. Medizintechnik Kg with 40% of records.

Which FDA product codes apply?

PFV (System, endovascular graft, arteriovenous (AV) dialysis acce), QWM (Stent Graft, Bypass, Superficial Femoral Artery)

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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