Straumann® Core Drill, left-hand cut for Service Set - FDA Registration CMDR-2025-04652A

Access comprehensive regulatory information for Straumann® Core Drill, left-hand cut for Service Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04652A and manufactured by Institut Straumann AG- Peter Merian-Weg 12, 4002 Basel, Switzerland Mfd. By: Straumann Villeret SA- Les Champs du Clos 2, CH-2613 Villeret, Switzerland in Switzerland. The device was registered on May 14, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Metro DNC Marketing 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.