AESCULAP TUNGSTEN CARBIDE-NEURO CUTTER - FDA Registration MDR-05345AK

Access comprehensive regulatory information for AESCULAP TUNGSTEN CARBIDE-NEURO CUTTER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05345AK and manufactured by Aesculap AG in Germany. The device was registered on October 25, 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.