A sterile non-bioabsorbable tubular device intended to be implanted in the lumen of the colon for the palliative treatment of colonic strictures caused by malignant neoplasms typically in the descending or sigmoid colon, or rectum. It is typically inserted and
| Company | Devices | Share |
|---|---|---|
| M.I.Tech Co., Ltd. | 30 | 51% |
| Boston Scientific Corporation | 18 | 31% |
| Taewoongmedical.Co.,Ltd | 8 | 14% |
| Cook Ireland Ltd | 3 | 5% |
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 |
|---|---|---|
| MQR | Stent, Colonic, Metallic, Expandable | 38 |
| MQR | STENT, COLONIC, METALIC, EXPANDABLE | 21 |
| MQR | Stent, colonic, metallic, expandable | 3 |
| MUM | STENT,METALLIC,EXPANDABLE,DUODENAL | 3 |
Use these as the dimensions to specify in a tender line.
59 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bare-metal colonic stent", from 4 companies. The largest labeler is M.I.Tech Co., Ltd. with 51% of records.
MQR (Stent, Colonic, Metallic, Expandable), MQR (STENT, COLONIC, METALIC, EXPANDABLE), MQR (Stent, colonic, metallic, expandable), MUM (STENT,METALLIC,EXPANDABLE,DUODENAL)
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.