Pajunk Sprotte Standard (with Introducer) - FDA Registration MDR-06479

Access comprehensive regulatory information for Pajunk Sprotte Standard (with Introducer) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06479 and manufactured by Pajunk GmbH Medizintechnologi Karl-Hall-Strasse 1, 78187, Geisingen, Germany in Germany. The device was registered on May 14, 2024.

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.