A sterile, thin, flexible, hollow tube percutaneously inserted into the jejunum, typically through puncture of the abdominal wall and stomach after distention of the gut by endoscopic methods. It is used to feed a patient who has a physical disability that pre
| Company | Devices | Share |
|---|---|---|
| Avanos Medical, Inc. | 644 | 97% |
| Corpak Medsystems, Inc. | 16 | 2% |
| Abbvie Inc. | 5 | 1% |
| Cook Incorporated | 1 | 0% |
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 |
|---|---|---|
| KNT | Tubes, gastrointestinal (and accessories) | 353 |
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) | 305 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 5 |
| KGC | TUBE, GASTRO-ENTEROSTOMY | 2 |
| KNY | ACCESSORIES, CATHETER, G-U | 1 |
Use these as the dimensions to specify in a tender line.
666 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Jejunostomy tube", from 4 companies. The largest labeler is Avanos Medical, Inc. with 97% of records.
KNT (Tubes, gastrointestinal (and accessories)), KNT (TUBES, GASTROINTESTINAL (AND ACCESSORIES)), KNT (Tubes, Gastrointestinal (And Accessories)), KGC (TUBE, GASTRO-ENTEROSTOMY)
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.