An implantable device intended to divert excessive cerebrospinal fluid (CSF) from the subarachnoid space of the lumbar spine to the peritoneal cavity where it can be absorbed into the body, as a treatment for raised CSF pressure (e.g., caused by hydrocephalus)
| Company | Devices | Share |
|---|---|---|
| Aesculap Ag | 30 | 45% |
| Medtronic Ps Medical, Inc. | 14 | 21% |
| Natus Medical Incorporated | 8 | 12% |
| Integra Lifesciences Production Corporation | 8 | 12% |
| Integra Lifesciences Corporation | 4 | 6% |
| Integra Lifesciences Switzerland Sàrl | 2 | 3% |
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 | 71 |
| JXG | Shunt, Central Nervous System And Components | 8 |
Use these as the dimensions to specify in a tender line.
66 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Lumboperitoneal shunt", from 6 companies. The largest labeler is Aesculap Ag with 45% 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.