Consulting Wallah › Device Explorer › Orthopaedic implants › Cerebrospinal fluid shunt valve
Device Explorer · FDA GUDID · GMDN 35965

Cerebrospinal fluid shunt valve

An implantable device intended to function as part of a lumboperitoneal, ventriculoperitoneal or ventriculoatrial shunt to regulate the pressure and flow level of cerebrospinal fluid (CSF) from the lumbar spine or brain to the peritoneum/heart right atrium in

US‑registered devices727in commercial distribution
Companies8labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription98%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Medtronic Ps Medical, Inc.21630%
Integra Lifesciences Production Corporation15221%
Aesculap Ag10214%
Christoph Miethke Gmbh & Co. Kg9813%
Integra Lifesciences Corporation558%
Natus Medical Incorporated537%
Sophysa274%
Integra Lifesciences Switzerland Sàrl243%

Top labelers

CompanyDevicesShare
Medtronic Ps Medical, Inc.21630%
Integra Lifesciences Production Corporation15221%
Aesculap Ag10214%
Christoph Miethke Gmbh & Co. Kg9813%
Integra Lifesciences Corporation558%
Natus Medical Incorporated537%
Sophysa274%
Integra Lifesciences Switzerland Sàrl243%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

M.BLUE PLUSM.BLUEPROGAV 2.0SHUNTASSISTANT 2.0GAV 2.0proGAV 2.0®miniNAV®proSA®PaediGAV®AESCULAPShuntAssistant®SophysaStrata®Strata®, BioGlide®StrataMR IIStrataMR

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

FDA product codes

CodeNameDevices
JXGShunt, central nervous system and components1,058
JXGShunt, Central Nervous System And Components53
HCACATHETER, VENTRICULAR6
MAJCatheter, percutaneous, intraspinal, short term2

GMDN & GCC registration

  • GMDN code 35965 · implantable
  • Single‑use 100% · sterile 100% · Rx‑only 98% · 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

Width (Millimeter) · 25Length (Centimeter) · 2

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

How many cerebrospinal fluid shunt valve products are registered in the US?

727 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cerebrospinal fluid shunt valve", from 8 companies. The largest labeler is Medtronic Ps Medical, Inc. with 30% of records.

Which FDA product codes apply?

JXG (Shunt, central nervous system and components), JXG (Shunt, Central Nervous System And Components), HCA (CATHETER, VENTRICULAR), MAJ (Catheter, percutaneous, intraspinal, short term)

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.

How do I get quotes?

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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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