SAMPLIX® TUBE K3E K3EDTA, LAVENDER CAP, NON-RIDGED - FDA Registration MDR-07746

Access comprehensive regulatory information for SAMPLIX® TUBE K3E K3EDTA, LAVENDER CAP, NON-RIDGED in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07746 and manufactured by Greiner Bio-One GmbH in Thailand. The device was registered on April 01, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Andaman Medical Philippines 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.