A collection of sterile and non-sterile devices intended to be used with an insufflation gas conditioning system and/or a laparoscopic gas distention system, or other gas source, to condition the insufflation gas stream [typically carbon dioxide (CO2)] by heat
| Company | Devices | Share |
|---|---|---|
| Deroyal Industries, Inc. | 39 | 50% |
| Surgical Direct, Inc. | 11 | 14% |
| Gri Medical & Electronic Technology Co., Ltd. | 8 | 10% |
| Bracco Diagnostics Inc. | 6 | 8% |
| Conmed Corporation | 5 | 6% |
| Karl Storz Gmbh & Co. Kg | 3 | 4% |
| Lexion Medical, Llc | 2 | 3% |
| Gimmi Gmbh | 1 | 1% |
| Gvs Filter Technology Uk Ltd | 1 | 1% |
| Integra Microfrance | 1 | 1% |
| Fisher & Paykel Healthcare Limited | 1 | 1% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| NKC | Tubing/tubing with filter, insufflation, laparoscopic | 63 |
| HIF | Insufflator, Laparoscopic | 9 |
| HIF | INSUFFLATOR, LAPAROSCOPIC | 6 |
| FCX | Insufflator, Automatic Carbon-Dioxide For Endoscope | 6 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 3 |
| HES | INSUFFLATOR, CARBON-DIOXIDE, UTEROTUBAL (AND ACCESSORIES) | 3 |
Use these as the dimensions to specify in a tender line.
78 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Insufflation gas conditioning tubing set", from 11 companies. The largest labeler is Deroyal Industries, Inc. with 50% of records.
NKC (Tubing/tubing with filter, insufflation, laparoscopic), HIF (Insufflator, Laparoscopic), HIF (INSUFFLATOR, LAPAROSCOPIC), FCX (Insufflator, Automatic Carbon-Dioxide 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.