PORTEX POLAR PREFORMED TRACHEAL TUBE - SOUTH ORAL UNCUFFED - FDA Registration DVR-7205

Access comprehensive regulatory information for PORTEX POLAR PREFORMED TRACHEAL TUBE - SOUTH ORAL UNCUFFED in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-7205 and manufactured by Smiths Medical International Ltd. in Mexico. The device was registered on April 02, 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.