A sharp bevel-edged, hollow tubular instrument designed for short-term use to withdraw a sample of cerebrospinal fluid (CSF), assist introduction of a spinal guidewire or catheter (e.g., lumboperitoneal shunt, intrathecal catheter), and/or deliver contrast med
| Company | Devices | Share |
|---|---|---|
| Pajunk Gmbh Medizintechnologie | 101 | 13% |
| Dr.Japan Co., Ltd. | 101 | 13% |
| Lccs Products Limited | 93 | 12% |
| Myco Medical Supplies Inc. | 70 | 9% |
| Becton, Dickinson And Company | 60 | 8% |
| Teleflex Incorporated | 42 | 6% |
| Icu Medical, Inc. | 39 | 5% |
| International Medical Development Corporation | 37 | 5% |
| Temena Gmbh | 33 | 4% |
| B. Braun Medical Inc. | 32 | 4% |
| Clint Pharmaceuticals, Inc. | 25 | 3% |
| Avid Medical, Inc. | 22 | 3% |
Company = labeler of record on GUDID. 34 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 |
|---|---|---|
| BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) | 620 |
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | 395 |
| MIA | NEEDLE, SPINAL, SHORT TERM | 59 |
| FMI | Needle, Hypodermic, Single Lumen | 20 |
| JXG | Shunt, central nervous system and components | 6 |
| CAZ | Anesthesia conduction kit | 5 |
Use these as the dimensions to specify in a tender line.
754 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Spinal needle, single-use", from 34 companies. The largest labeler is Pajunk Gmbh Medizintechnologie with 13% of records.
BSP (NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)), BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)), MIA (NEEDLE, SPINAL, SHORT TERM), FMI (Needle, Hypodermic, Single Lumen)
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.