Trokabone (with Sternal)Pajunk Bone Biopsy Puncture System - FDA Registration MDR-06323 B

Access comprehensive regulatory information for Trokabone (with Sternal)Pajunk Bone Biopsy Puncture System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06323 B and manufactured by Pajunk GmbH Medizintechnologie - Karl - Hall - Strasse 1, 78187 Geisingen Germany in Germany. The device was registered on June 23, 2025.

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