A sterile, 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
| Company | Devices | Share |
|---|---|---|
| Fhc, Inc. | 41 | 76% |
| Clearpoint Neuro, Inc. | 11 | 20% |
| Surgix Medical Llc | 1 | 2% |
| Katalyst Surgical Llc | 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 |
|---|---|---|
| HAW | Neurological stereotaxic Instrument | 41 |
| HCD | Cannula, Ventricular | 10 |
| GZL | ELECTRODE, DEPTH | 6 |
| SDG | Brain Intraparenchymal Infusion Cannula | 2 |
| HAO | INSTRUMENT, SURGICAL, NON-POWERED | 2 |
| HAO | Instrument, Surgical, Non-Powered | 1 |
Use these as the dimensions to specify in a tender line.
54 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intracerebral cannula, nonimplantable, single-use", from 4 companies. The largest labeler is Fhc, Inc. with 76% of records.
HAW (Neurological stereotaxic Instrument), HCD (Cannula, Ventricular), GZL (ELECTRODE, DEPTH), SDG (Brain Intraparenchymal Infusion Cannula)
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.
Add intracerebral cannula, nonimplantable, single-use to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.
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.