BIOTEQ® PRECISION INFUSION SET, AIR-VENTED SPIKE WITHOUT Y-CONNECTOR - FDA Registration MDR-05796L

Access comprehensive regulatory information for BIOTEQ® PRECISION INFUSION SET, AIR-VENTED SPIKE WITHOUT Y-CONNECTOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05796L and manufactured by Bioteque Medical Phil. Inc. in Philippines. The device was registered on December 10, 2018.

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