Consulting Wallah › Device Explorer › Cardiovascular › Cardiovascular embolization implantation kit
Device Explorer · FDA GUDID · GMDN 64358

Cardiovascular embolization implantation kit

A collection of dedicated instruments intended to be used for the implantation of an embolization implant (implant not included). It typically includes devices for arterial access (e.g., needle, introducer, guidewires) and devices to assist introduction and po

US‑registered devices201in commercial distribution
Companies1labelers 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, Llc201100%

Top labelers

CompanyDevicesShare
Cardinal Health 200, Llc201100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CARDINAL HEALTH

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

FDA product codes

CodeNameDevices
OJGNeurological tray167
OEZCardiovascular procedure kit31
LROGeneral surgery tray (kit)2
OEZCardiovascular Procedure Kit1
OJHOrthopedic tray1

GMDN & GCC registration

  • GMDN code 64358 · 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

No structured size data on the register.

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

How many cardiovascular embolization implantation kit products are registered in the US?

201 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiovascular embolization implantation kit", from 1 companies. The largest labeler is Cardinal Health 200, Llc with 100% of records.

Which FDA product codes apply?

OJG (Neurological tray), OEZ (Cardiovascular procedure kit), LRO (General surgery tray (kit)), OEZ (Cardiovascular Procedure Kit)

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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