Vacuette® Tube K2E K2EDTA Lavender Cap-white ring, PREMIUM - FDA Registration IVDR-00999 D

Access comprehensive regulatory information for Vacuette® Tube K2E K2EDTA Lavender Cap-white ring, PREMIUM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00999 D and manufactured by Greiner Bio-One GmbH- Bad Haller Str. 32, 4550 Kremsmünster, Österreich Mfd. By: Greiner Bio-One (Thailand) Ltd.- 700/172 Moo. 1, Tambon Bankao, Amphur Phanthong Chonburi 20160, Thailand in Thailand. The device was registered on July 10, 2026.

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.