PORTEX TUOHY NEEDLE

Access comprehensive regulatory information for PORTEX TUOHY NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-2370 and manufactured by Smiths Medical International Ltd. in Mexico. The device was registered on January 22, 2019.

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.