CRANIOFIX 2 TITANIUM CLAMP - FDA Registration DVR-8536

Access comprehensive regulatory information for CRANIOFIX 2 TITANIUM CLAMP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8536 and manufactured by Aesculap AG in Germany. The device was registered on November 12, 2018.

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.