SonoPlex® II Facet Sprotte Nerve-Locating Anesthesia Needle - FDA Registration CMDR-2025-03698C

Access comprehensive regulatory information for SonoPlex® II Facet Sprotte Nerve-Locating Anesthesia Needle in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03698C and manufactured by Pajunk GmbH Medizintechnologie Karl-hall-Str. 1, 78187 Geisingen, Germany in Germany. The device was registered on January 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.