SCARBAN® LIGHT SILICONE BANDAGE - FDA Registration MDR-08631

Access comprehensive regulatory information for SCARBAN® LIGHT SILICONE BANDAGE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08631 and manufactured by BAP Medical B.V. - Apeldoorn, The Netherlands mfd. By: Scarpro N.V. - Aalter, Belgium in Belgium. The device was registered on September 23, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (EG Healthcare 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.