Surgical Sponge - ANVISA Registration 80420209013

Access comprehensive regulatory information for Surgical Sponge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80420209013 and manufactured by VIDI MEDIKAL TEKNIK. The registration is held by VISION LINE IMPORTAÇÃO E COMÉRCIO DE MATERIAIS E EQUIPAMENTOS MÉDICOS LTDA-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including G. SURGIWEAR LIMITED, Tecfen Medical, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.