BD MAX™ UVE SPECIMEN COLLECTION KIT - FDA Registration MDR-09654

Access comprehensive regulatory information for BD MAX™ UVE SPECIMEN COLLECTION KIT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09654 and manufactured by Becton Dickinson Holdings Pte. Ltd. in USA. The device was registered on May 13, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Patient Care 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.