ENDOTAK RELIANCE SG 4-SITE (ACTIVE) QUADRIPOLAR DEFIBRILLATOR LEAD - FDA Registration MDR-01717

Access comprehensive regulatory information for ENDOTAK RELIANCE SG 4-SITE (ACTIVE) QUADRIPOLAR DEFIBRILLATOR LEAD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01717 and manufactured by Boston Scientific Corporation in USA. The device was registered on March 18, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific Phils., Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.