PORTEX ULTRAPERC PERCUATANEOUS DILATATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCER WITHOUT TRACHEOSTOMY TUBE - FDA Registration MDR-01833

Access comprehensive regulatory information for PORTEX ULTRAPERC PERCUATANEOUS DILATATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCER WITHOUT TRACHEOSTOMY TUBE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01833 and manufactured by Smiths Medical International Ltd. in Czech Republic. The device was registered on April 29, 2020.

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.