Vilowond® Gauze & Vilowond® Nonwoven - EUDAMED Registration 06221329007035

Access comprehensive regulatory information for Vilowond® Gauze & Vilowond® Nonwoven in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 06221329007035 and manufactured by Pharmaplast in Egypt.

This page provides complete registration details including trade name (Vilowond®Gauze Non-Sterile), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.