TECHNOWOOD SSS GUIDEWIRE ANGIOGRAPHIC GUIDEWIRE - FDA Registration DVR-5722

Access comprehensive regulatory information for TECHNOWOOD SSS GUIDEWIRE ANGIOGRAPHIC GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5722 and manufactured by Technowood Manufacturing Corporation in Philippines. The device was registered on January 03, 2019.

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