Consulting Wallah › Device Explorer › Procedure kits & trays › Neurosurgical procedure kit, non-medicated, single
Device Explorer · FDA GUDID · GMDN 44063

Neurosurgical procedure kit, non-medicated, single-use

A collection of various sterile neurosurgical instruments, dressings and the necessary materials used to perform a neurosurgical procedure. It does not contain pharmaceuticals. This is a single-use device.

US‑registered devices11,623in commercial distribution
Companies28labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Cardinal Health 200, Llc11,37698%
Aligned Medical Solutions470%
Medtronic, Inc.430%
Nico Corporation330%
Avanos Medical, Inc.180%
Nalu Medical, Inc.170%
Greatbatch Ltd140%
Bioplate, Inc.130%

Top labelers

CompanyDevicesShare
Cardinal Health 200, Llc11,37698%
Aligned Medical Solutions470%
Medtronic, Inc.430%
Nico Corporation330%
Avanos Medical, Inc.180%
Nalu Medical, Inc.170%
Greatbatch Ltd140%
Bioplate, Inc.130%
St. Jude Medical, Inc.80%
Acra-Cut Inc80%
Saluda Medical Pty Limited60%
Spinal Modulation, Inc.50%

Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

mild Device KitOptaBlateNAAxium™SJM™coflex single-use instrumentsBIOTRONIKCARDINAL HEALTH"13G Tuohy Needle 4.5"""Guidewire 3-Pack"13G Tuohy Needle 6"""IntraceptSilicone Cap for LSB Anchor BoltLead Cover - Box of 12Placement Stay FlangeAlgovita®

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
OJGNeurological tray11,352
OJGNeurological Tray333
LGWSTIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF41
QRBStimulator, spinal-cord, totally implanted for relief of pai29
GZBStimulator, Spinal-Cord, Implanted (Pain Relief)29
OJHOrthopedic tray27

GMDN & GCC registration

  • GMDN code 44063 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 57Length (Inch) · 7Needle Gauge (Gauge) · 7

Use these as the dimensions to specify in a tender line.

How many neurosurgical procedure kit, non-medicated, single-use products are registered in the US?

11,623 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Neurosurgical procedure kit, non-medicated, single-use", from 28 companies. The largest labeler is Cardinal Health 200, Llc with 98% of records.

Which FDA product codes apply?

OJG (Neurological tray), OJG (Neurological Tray), LGW (STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF), QRB (Stimulator, spinal-cord, totally implanted for relief of pai)

Is this the same as UAE/GCC registration?

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.

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