Saudi Arabia SFDA registration ME0000000975SFDAA00091
Ultimaster Sirolimus Eluting Coronary Stent System
Saudi Arabia·Medical Device·Terumo Europe N.V.·Class IIIActiveProduct information
Implantable drug eluting coronary artery stent
Product use
Ultimaster sirolimus eluting coronary stent system is indicated for improving myocardial blood flow in patients with stenotic lesions in coronary arteries with a reference vessel diameter between 2.5 mm and 4.0 mm and up to 25 mm in length
Device classification
- Risk Class
- Class III
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000975SFDAA00091
- Authorization ID
- GHTF-2014-0108
- Status
- Active
- Expire Date
- December 18, 2016
Manufacturer
- Manufacturer Name
- Terumo Europe N.V.
Product accessories
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About this record
Access comprehensive regulatory information for Ultimaster Sirolimus Eluting 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 ME0000000975SFDAA00091 and manufactured by Terumo Europe N.V..
This page provides complete registration details including product category (Medical Device), manufacturer information, 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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