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Device Explorer · FDA GUDID · GMDN 44856

Cerebrospinal fluid shunt valve programmer

A device intended to noninvasively modify the operating pressure of a programmable, non-active, implanted hydrocephalic valve that will be part of a hydrocephalic shunt system. It is used in neurosurgery for intra- and postoperative treatment of hydrocephalus

US‑registered devices66in commercial distribution
Companies6labelers on GUDID
Single‑use2%of device records
Sterile5%labelled sterile
Prescription85%Rx‑only share
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Share of device records

Medtronic Ps Medical, Inc.2335%
Christoph Miethke Gmbh & Co. Kg2030%
Sophysa1015%
Integra Lifesciences Production Corporation69%
Aesculap Ag58%
Integra Lifesciences Switzerland Sàrl23%

Top labelers

CompanyDevicesShare
Medtronic Ps Medical, Inc.2335%
Christoph Miethke Gmbh & Co. Kg2030%
Sophysa1015%
Integra Lifesciences Production Corporation69%
Aesculap Ag58%
Integra Lifesciences Switzerland Sàrl23%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

M.BLUEM.BLUE PLUSproGAV 2.0®proSA®proGAV®Polaris valves electronic reading instrumentSophysaStrataVarius®Strata®StrataVariusStrata II Adjustment KitStrataMR™StrataMRStrata™STRATA®N/A

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 components81
JXGShunt, Central Nervous System And Components1

GMDN & GCC registration

  • GMDN code 44856 · non‑implantable
  • Single‑use 2% · sterile 5% · Rx‑only 85% · 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

No structured size data on the register.

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

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

66 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cerebrospinal fluid shunt valve programmer", from 6 companies. The largest labeler is Medtronic Ps Medical, Inc. with 35% of records.

Which FDA product codes apply?

JXG (Shunt, central nervous system and components), JXG (Shunt, Central Nervous System And Components)

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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