A flexible tube intended for percutaneous introduction into two or more abdominothoracic anatomies (nephrostomy, biliary, abscess, pleural, peritoneal, mediastinal) [i.e., multi-purpose] for intermittent or long-term drainage. It is available in various design
| Company | Devices | Share |
|---|---|---|
| Mermaid Medical A/S | 81 | 28% |
| Cook Incorporated | 80 | 28% |
| Argon Medical Devices, Inc. | 41 | 14% |
| B Braun Interventional Systems, Inc | 38 | 13% |
| Teleflex Incorporated | 32 | 11% |
| Rocket Medical Plc | 4 | 1% |
| H.S. Hospital Service Spa | 4 | 1% |
| Gcmedica Enterprise Ltd.(Wuxi) | 2 | 1% |
| Boston Scientific Corporation | 2 | 1% |
| Rand Spa | 1 | 0% |
| Cardinal Health 200, Llc | 1 | 0% |
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 |
|---|---|---|
| FGE | Catheter, Biliary, Diagnostic | 80 |
| LJE | CATHETER, NEPHROSTOMY | 77 |
| GBO | CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY | 44 |
| FGE | Stents, drains and dilators for the biliary ducts | 38 |
| GBO | Catheter, Nephrostomy, General & Plastic Surgery | 33 |
| GBZ | CATHETER, CHOLANGIOGRAPHY | 32 |
Use these as the dimensions to specify in a tender line.
286 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Multi-purpose percutaneous abdominothoracic drainage catheter", from 11 companies. The largest labeler is Mermaid Medical A/S with 28% of records.
FGE (Catheter, Biliary, Diagnostic), LJE (CATHETER, NEPHROSTOMY), GBO (CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY), FGE (Stents, drains and dilators for the biliary ducts)
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.