PORTEX® BLUE LINE ULTRA® TRACHEOSTOMY TUBE INNER CANNULA - FDA Registration MDR-04517

Access comprehensive regulatory information for PORTEX® BLUE LINE ULTRA® TRACHEOSTOMY TUBE INNER CANNULA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04517 and manufactured by Smiths Medical Czech Republic A.S. in Czech Republic. The device was registered on June 30, 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.