A slender, sharply-pointed metal tube designed to introduce or remove gas from the peritoneal cavity as a therapeutic or surgical/radiological procedural method. It is often inserted into the peritoneal cavity for the purpose of insufflation [e.g., with carbon
| Company | Devices | Share |
|---|---|---|
| Applied Medical Resources Corporation | 23 | 28% |
| Teleflex Incorporated | 6 | 7% |
| Conmed Corporation | 6 | 7% |
| Purple Surgical International Limited | 4 | 5% |
| Deroyal Industries, Inc. | 4 | 5% |
| American Medical Endoscopy, Inc. | 3 | 4% |
| Ethicon Endo-Surgery, Llc | 3 | 4% |
| Unimicro Medical Systems (Shenzhen) Co., Ltd. | 2 | 2% |
| Guangzhou T.K Medical Instrument Co.,Ltd. | 2 | 2% |
| Safeguard Medical Technologies Limited | 2 | 2% |
| Unimax Medical Systems Inc. | 2 | 2% |
| Advanced Medical Design Co., Ltd. | 2 | 2% |
Company = labeler of record on GUDID. 24 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 |
|---|---|---|
| HET | Laparoscope, Gynecologic (And Accessories) | 28 |
| GCJ | Laparoscope, General & Plastic Surgery | 26 |
| FZP | Clip, Implantable | 23 |
| MDM | Instrument, Manual, Surgical, General Use | 23 |
| FHO | Pneumoperitoneum Needle | 16 |
| HIF | Insufflator, Laparoscopic | 12 |
Use these as the dimensions to specify in a tender line.
81 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Spring-loaded pneumoperitoneum needle, single-use", from 24 companies. The largest labeler is Applied Medical Resources Corporation with 28% of records.
HET (Laparoscope, Gynecologic (And Accessories)), GCJ (Laparoscope, General & Plastic Surgery), FZP (Clip, Implantable), MDM (Instrument, Manual, Surgical, General Use)
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.