BIOTEQ® Precision Infusion Set, Air-Vented Spike, Needleless Type Y-Connector, DEHP - FDA Registration MDR-05796I

Access comprehensive regulatory information for BIOTEQ® Precision Infusion Set, Air-Vented Spike, Needleless Type Y-Connector, DEHP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05796I and manufactured by Block 14, Lot 2,3,4, Hermosa Ecozone Industrial Park, Brgy. Palihan, Hermosa, Bataan in Philippines. The device was registered on May 20, 2025.

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