VACUETTE® VISIO PLUS NEEDLE - FDA Registration MDR-06518

Access comprehensive regulatory information for VACUETTE® VISIO PLUS NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06518 and manufactured by Greiner Bio-One GmbH Bad Haller Str. 32 4550 Kremsmunster, Austria Mfd By: Nipro Medical Industries Ltd. - Tatebayashi Plant, 2-19-64, Matsubara, Tatebayashi-shi, Gunma, 374-8518 Japan in Austria. The device was registered on May 14, 2024.

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.