PORTEX EPIDURAL MINIPACK SYSTEM 1 - FDA Registration MDR-05034

Access comprehensive regulatory information for PORTEX EPIDURAL MINIPACK SYSTEM 1 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05034 and manufactured by Smiths Medical International Ltd. in United Kingdom. The device was registered on December 11, 2017.

This page provides complete registration details including manufacturer information, importer/distributor details (Rebmann, 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.