Vacutest Sodium Citrate 3.2% Blood Collection - FDA Registration MDR-05519

Access comprehensive regulatory information for Vacutest Sodium Citrate 3.2% Blood Collection in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05519 and manufactured by Vacutest Kima S.R.L. Via dell' Industria, 12-35020 Arzergrande (Pd) Italy in Italy. The device was registered on May 28, 2024.

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