RADIFOCUS GLIDECATH ANGIOGRAPHIC CATHETER - SFDA Registration ME0000000975SFDAA00161
Access comprehensive regulatory information for RADIFOCUS GLIDECATH ANGIOGRAPHIC CATHETER 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 ME0000000975SFDAA00161 and manufactured by Terumo Europe N.V..
This page provides complete registration details including product category (MD), 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.
Angiography Catheter
The RADIFOCUS GLIDECATH is a sterile and for single use catheter, intended for use in angiographic procedures. It delivers radiopaque media and therapeutic agents to selected sites in the vascular system. It is also used to lead a guide wire or a catheter into the target site.
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