Graft Preparation System - ANVISA Registration 10343659014

Access comprehensive regulatory information for Graft Preparation System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10343659014 and manufactured by HUMAN BRAIN WAVE SRL. The registration is held by SKINTEC COMERCIAL IMP. E EXP. LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including HUMAN BRAIN WAVE SRL, NEXGEN IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MEDICOS E VETERINARIOS 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.