A non-bioabsorbable, tubular device made of metal intended to be implanted in a peripheral (typically the iliac and/or femoral) vein to maintain patency in patients with constrained venous outflow; it is not intended for coronary or intracranial venous stentin
| Company | Devices | Share |
|---|---|---|
| Angiomed Gmbh & Co. Medizintechnik Kg | 84 | 59% |
| Medtronic, Inc. | 31 | 22% |
| Cook Ireland Ltd | 28 | 20% |
Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| QAN | Stent, iliac vein | 161 |
| QAN | Stent, Iliac Vein | 14 |
Use these as the dimensions to specify in a tender line.
143 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bare-metal peripheral venous stent", from 3 companies. The largest labeler is Angiomed Gmbh & Co. Medizintechnik Kg with 59% of records.
QAN (Stent, iliac vein), QAN (Stent, Iliac Vein)
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.