BIOTEQ® NASAL OXYGEN CANNULA - FDA Registration MDR-09764A

Access comprehensive regulatory information for BIOTEQ® NASAL OXYGEN CANNULA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09764A and manufactured by Bioteque Medical Phil. Inc. in Philippines. The device was registered on June 16, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Bioteque Medical Phil. 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.