RADIOPAQUE GLASS IONOMER POSTERIOR RESTORATIVE CEMENT - FDA Registration MDR-07483

Access comprehensive regulatory information for RADIOPAQUE GLASS IONOMER POSTERIOR RESTORATIVE CEMENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07483 and manufactured by Medicept UK Ltd. - 2nd Flr., Hygeia House, 66 College Road, Harrow, Middlesex HAI, IBE, United Kingdom mfd. by: Medicept Dental India Pvt. Ltd. - Unit No. 207, 208, 209, Bldg. No. F-8, Bhumi World Industrial Park, Mumbai Nashik Expressway, Pimplas, Bhiwandi, Thane, Mumbai 421 302 Maharashtra, India in India. The device was registered on April 23, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Surgicom Trading Corporation), 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.