Straumann® PURE Ceramic Implant Monotype, ZrO2, ND, ZLA® - FDA Registration CMDR-2023-01370A

Access comprehensive regulatory information for Straumann® PURE Ceramic Implant Monotype, ZrO2, ND, ZLA® in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01370A and manufactured by Institut Straumann AG - Peter-Merian-Weg 12, 4002, Basel, Switzerland Mfd. By: Straumann Villeret SA - Les Champd du Clos 2, CH - 2613 Villeret, Switzerland in Switzerland. The device was registered on March 14, 2023.

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.