STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET - FDA Registration MDR-09833A

Access comprehensive regulatory information for STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09833A and manufactured by Transmedic Pte. Ltd. in Germany. The device was registered on April 20, 2022.

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