An implantable device intended to create a fluid path connection between components of a cerebrospinal fluid (CSF) shunt assembly (e.g., lumbar and/or peritoneal catheters of a ventriculoperitoneal or lumboperitoneal shunt), designed to remove excess cerebrosp
| Company | Devices | Share |
|---|---|---|
| Integra Lifesciences Production Corporation | 22 | 25% |
| Natus Medical Incorporated | 18 | 21% |
| Christoph Miethke Gmbh & Co. Kg | 17 | 20% |
| Medtronic Ps Medical, Inc. | 14 | 16% |
| Sophysa | 9 | 10% |
| Integra Lifesciences Corporation | 7 | 8% |
Company = labeler of record on GUDID. 6 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 |
|---|---|---|
| JXG | Shunt, central nervous system and components | 98 |
| JXG | Shunt, Central Nervous System And Components | 18 |
Use these as the dimensions to specify in a tender line.
87 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cerebrospinal fluid shunt connector", from 6 companies. The largest labeler is Integra Lifesciences Production Corporation with 25% of records.
JXG (Shunt, central nervous system and components), JXG (Shunt, Central Nervous System And Components)
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.