Pajunk Epilong Anesthesia Kit, Epidural - FDA Registration MDR-06263I

Access comprehensive regulatory information for Pajunk Epilong Anesthesia Kit, Epidural in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06263I and manufactured by Pajunk GmbH Medizintechnologie Karl-Hall-Str. 1, 78187 Geisingen, Germany in Germany. The device was registered on January 09, 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.