ARROW-CLARK™ VECTORFLOW™ ANTEGRADE HEMODIALYSIS CATHETERIZATION SET - FDA Registration MDR-08019

Access comprehensive regulatory information for ARROW-CLARK™ VECTORFLOW™ ANTEGRADE HEMODIALYSIS CATHETERIZATION SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08019 and manufactured by Teleflex Medical in USA. The device was registered on June 10, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (IDS Medical Systems Philippines, 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.