Gel - ANVISA Registration 81505600003

Access comprehensive regulatory information for Gel in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81505600003 and manufactured by BIOPLAX LIMITED. The registration is held by MR PHARMA LTDA 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 RMC - INDÚSTRIA BRASILEIRA DE PRODUTOS MÉDICOS LTDA, HELIANTO FARMACEUTICA LTDA, 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.