Adult VAD Tubing Pack (For Use with CentriMag™) - FDA Registration CMDR-2025-03745

Access comprehensive regulatory information for Adult VAD Tubing Pack (For Use with CentriMag™) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03745 and manufactured by Transmedic Pte. Ltd. in Singapore. The device was registered on January 31, 2025.

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.