Consulting Wallah › Device Explorer › Other devices › Cranial port/reservoir
Device Explorer · FDA GUDID · GMDN 61375

Cranial port/reservoir

A sterile, implantable chamber intended to be connected to an intracerebral catheter for infusion/injection of materials (e.g., chemotherapeutic agents, radioisotopes) into the brain (e.g., cerebral ventricles, cystic tumours, tumour cavities); it may also be

US‑registered devices203in commercial distribution
Companies7labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Medtronic Ps Medical, Inc.11858%
Christoph Miethke Gmbh & Co. Kg3115%
Integra Lifesciences Production Corporation2412%
Natus Medical Incorporated126%
Medtronic Powered Surgical Solutions84%
Aesculap Ag63%
Micro Therapeutics, Inc.42%

Top labelers

CompanyDevicesShare
Medtronic Ps Medical, Inc.11858%
Christoph Miethke Gmbh & Co. Kg3115%
Integra Lifesciences Production Corporation2412%
Natus Medical Incorporated126%
Medtronic Powered Surgical Solutions84%
Aesculap Ag63%
Micro Therapeutics, Inc.42%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

AESCULAPReservoirN/ANANatus®CODMAN® ACCU-FLO®CODMAN® HOLTER® SALMON™-RICKHAM®CODMAN® HOLTER®CODMAN® HOLTER® RICKHAM®CODMAN® HOLTER® SELKER

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 components181
LKGPort & catheter, implanted, subcutaneous, intraventricular26
LKGPORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR24
JXGShunt, Central Nervous System And Components12
KGXTape and bandage, adhesive1
DSFRECORDER, PAPER CHART1

GMDN & GCC registration

  • GMDN code 61375 · 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) · 54Width (Millimeter) · 16

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

How many cranial port/reservoir products are registered in the US?

203 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cranial port/reservoir", from 7 companies. The largest labeler is Medtronic Ps Medical, Inc. with 58% of records.

Which FDA product codes apply?

JXG (Shunt, central nervous system and components), LKG (Port & catheter, implanted, subcutaneous, intraventricular), LKG (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR), 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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