Saudi Arabia SFDA registration ME0000000975SFDAA00155
KANAME CoCr CORONARY STENT SYSTEM
Saudi Arabia·Medical Device·Terumo Europe N.V.·Class IIIActiveProduct 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
Product accessories
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About this record
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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