SKIPER EUROSETS™ OXYGENATOR - FDA Registration MDR-02960

Access comprehensive regulatory information for SKIPER EUROSETS™ OXYGENATOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-02960 and manufactured by Eurosets S.R.L. in Italy. The device was registered on December 15, 2016.

This page provides complete registration details including manufacturer information, importer/distributor details (Technowood Manufacturing Corporation), 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.