Graft Preparation System - ANVISA Registration 10343650061

Access comprehensive regulatory information for Graft Preparation System in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10343650061 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 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.