Kimatest Microtest K3 EDTA Blood Collection Tube - FDA Registration MDR-05146

Access comprehensive regulatory information for Kimatest Microtest K3 EDTA Blood Collection Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05146 and manufactured by Vacutest Kima S.R.L- Via dell' Industria, 12-35020 Arzergrande (PD) Italy Mfd by: MEUS S.R.L- Via Leonardo da Vinci, 24B- 26- 28- Zona Industriale Tognana- 35028 Piove di Sacco (PD) Italy in Italy. The device was registered on June 10, 2025.

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.