A nonimplantable, rigid tube intended to be surgically inserted through the skull to access the brain (e.g., cerebral ventricles) for cerebrospinal fluid (CSF) drainage, infusion of materials, and/or for use as a port through which instruments, leads and/or pr
| Company | Devices | Share |
|---|---|---|
| Fhc, Inc. | 24 | 48% |
| Integra Lifesciences Production Corporation | 24 | 48% |
| Hayden Medical, Inc. | 1 | 2% |
| Steris Corporation | 1 | 2% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| HAO | INSTRUMENT, SURGICAL, NON-POWERED | 39 |
| HAW | Neurological stereotaxic Instrument | 23 |
| HCD | Cannula, ventricular | 7 |
| HCA | CATHETER, VENTRICULAR | 4 |
| HBA | Neurosurgical paddie | 2 |
| GZL | ELECTRODE, DEPTH | 1 |
Use these as the dimensions to specify in a tender line.
50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intracerebral cannula, nonimplantable, reusable", from 4 companies. The largest labeler is Fhc, Inc. with 48% of records.
HAO (INSTRUMENT, SURGICAL, NON-POWERED), HAW (Neurological stereotaxic Instrument), HCD (Cannula, ventricular), HCA (CATHETER, VENTRICULAR)
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.