A collection of flexible tubing intended to channel medical gas [e.g., carbon dioxide (CO2), medical air] from its source into a body cavity for insufflation during endoscopy (e.g., gastrointestinal endoscopy, laparoscopy, arthroscopy). It includes synthetic p
| Company | Devices | Share |
|---|---|---|
| Yangzhou Fartley Medical Instrument Technology Co., Ltd | 30 | 12% |
| Ga Health Company Limited | 25 | 10% |
| Medivators Inc. | 20 | 8% |
| Josnoe Medical, Inc. | 15 | 6% |
| Canadian Hospital Specialties Limited | 15 | 6% |
| Erbe Medical, Llc | 14 | 6% |
| W.O.M. World Of Medicine Gmbh | 14 | 6% |
| Northgate Technologies Inc. | 12 | 5% |
| Techmedical Services, Inc. | 10 | 4% |
| Micro-Tech Usa | 8 | 3% |
| Conmed Corporation | 8 | 3% |
| Keymed (Medical & Industrial Equipment) Limited | 8 | 3% |
Company = labeler of record on GUDID. 33 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 |
|---|---|---|
| OCX | Endoscopic Irrigation/Suction System | 78 |
| NKC | Tubing/Tubing With Filter, Insufflation, Laparoscopic | 58 |
| HIF | Insufflator, Laparoscopic | 44 |
| FEQ | PUMP, AIR, NON-MANUAL, FOR ENDOSCOPE | 41 |
| NKC | Tubing/tubing with filter, insufflation, laparoscopic | 30 |
| FAJ | Cystoscope And Accessories, Flexible/Rigid | 23 |
Use these as the dimensions to specify in a tender line.
246 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endoscopic insufflation tubing set, single-use", from 33 companies. The largest labeler is Yangzhou Fartley Medical Instrument Technology Co., Ltd with 12% of records.
OCX (Endoscopic Irrigation/Suction System), NKC (Tubing/Tubing With Filter, Insufflation, Laparoscopic), HIF (Insufflator, Laparoscopic), FEQ (PUMP, AIR, NON-MANUAL, FOR ENDOSCOPE)
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.