Polaris™ Loop - SFDA Registration ME0000000537SFDAA00324
Access comprehensive regulatory information for Polaris™ Loop in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000000537SFDAA00324 and manufactured by Boston Scientific Corporation.
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.
Polymeric Ureteral Stent
The Polaris Loop Ureteral Stents are intended to facilitate drainage from the kidney to the bladder via placement endoscopically, fluoroscopically, or during an open surgical procedure by a trained physician.
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