A non-bioabsorbable tubular device intended to be implanted in the aorta to maintain aortic patency and improve luminal diameter, typically in patients with symptomatic atherosclerotic disease or recurrent coarctation (narrowing) of the aorta. It is a metallic
| Company | Devices | Share |
|---|---|---|
| B Braun Interventional Systems, Inc | 191 | 91% |
| Artivion, Inc. | 10 | 5% |
| William Cook Europe Aps | 6 | 3% |
| Renata Medical, Inc. | 2 | 1% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| PNF | Aortic stent | 191 |
| QSK | Hybrid Stent Graft, Thoracic Aortic Lesion Treatment | 10 |
| MIH | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | 6 |
| PNF | Aortic Stent | 2 |
| QWC | Pulmonary Stent | 2 |
Use these as the dimensions to specify in a tender line.
209 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bare-metal aortic stent", from 4 companies. The largest labeler is B Braun Interventional Systems, Inc with 91% of records.
PNF (Aortic stent), QSK (Hybrid Stent Graft, Thoracic Aortic Lesion Treatment), MIH (SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT), PNF (Aortic Stent)
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.