Percuflex™ - SFDA Registration ME0000000537SFDAA00315
Access comprehensive regulatory information for Percuflex™ 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 ME0000000537SFDAA00315 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 Ureteral Stent is intended to facilitate drainage from the kidney to the bladder via placement endoscopically or fluoroscopically by a trained physician.
[]