VACUETTE TUBE FE SODIUM FLUORIDE / K3EDTA, PREMIUM - FDA Registration MDR-10342A

Access comprehensive regulatory information for VACUETTE TUBE FE SODIUM FLUORIDE / K3EDTA, PREMIUM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10342A and manufactured by Greiner Bio-One GmbH in Thailand. The device was registered on September 22, 2020.

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