PulseCath® Percutaneous Ventricular Assist Device - FDA Registration CMDR-2025-04083`

Access comprehensive regulatory information for PulseCath® Percutaneous Ventricular Assist Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04083` and manufactured by Pulsecath B.V. De Corridor 5, 3621 ZA, Breukelen, The Netherlands in The Netherlands. The device was registered on March 03, 2025.

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