A sterile, implantable tube intended to be surgically placed in a specific area of the brain (e.g., basal ganglia) to position a deep brain electrical stimulation lead/electrode, using a stereotactic surgery system, and to function as a guide for subsequent an
| Company | Devices | Share |
|---|---|---|
| Fhc, Inc. | 117 | 60% |
| Alpha Omega Engineering Co. Ltd. | 78 | 40% |
Company = labeler of record on GUDID. 2 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 |
|---|---|---|
| HAW | Neurological stereotaxic Instrument | 132 |
| GZL | Electrode, Depth | 79 |
| HAO | INSTRUMENT, SURGICAL, NON-POWERED | 3 |
| GZL | ELECTRODE, DEPTH | 2 |
Use these as the dimensions to specify in a tender line.
195 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intracerebral cannula, implantable", from 2 companies. The largest labeler is Fhc, Inc. with 60% of records.
HAW (Neurological stereotaxic Instrument), GZL (Electrode, Depth), HAO (INSTRUMENT, SURGICAL, NON-POWERED), GZL (ELECTRODE, DEPTH)
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.