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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.

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Class III
ME0000000975SFDAA00155
KANAME CoCr CORONARY STENT SYSTEM
SFDA Registration: ME0000000975SFDAA00155
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Product Information

Implantable Cobalt-Chromium Stent

Product Use

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

Device Classification
Risk Class
Class III
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000975SFDAA00155
Authorization ID
GHTF-2015-0209
Status
Active
Expire Date
December 18, 2016
Manufacturer
Manufacturer Name
Terumo Europe N.V.
Model Information
Model ID(s)
CS-RD2509KW CS-RD2512KW CS-RD2515KW CS-RD2518KW CS-RD2524KW CS-RD2528KW CS-RD2709KW CS-RD2712KW CD-RD2715KW CS-RD2718KW CS-RD2724KW CS-RD2728KW CS-RD3009KW CS-RD3012KW CS-RD3015KW CS-RD3018KW CS-RD3024KW CS-RD3028KW CS-RD3509KW CS-RD3512KW CS-RD3515KW CS-RD3518KW CS-RD3524KW CS-RD3528KW CS-RD4009KW CS-RD4012KW CS-RD4015KW CS-RD4018KW CS-RD4024KW CS-RD4028KW
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