KANAME CoCr CORONARY STENT SYSTEM - SFDA Registration ME0000000975SFDAA00155
Access comprehensive regulatory information for KANAME CoCr CORONARY STENT SYSTEM in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000975SFDAA00155 and manufactured by Terumo Europe N.V..
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Implantable Cobalt-Chromium Stent
Intended to reach stenotic lesions in coronary arteries via a rapid exchange balloon delivery system and intended to improve myocardial blood flow in patients with stenotic lesions in coronary arteries
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