FIBRONECTIN - ANVISA Registration 10237610065

Access comprehensive regulatory information for FIBRONECTIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10237610065 and manufactured by HOLOGIC INC.. The registration is held by KOLPLAST CI 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, 3 companies making the same product including ACRO BIOTECH, INC. (MONTCLAIR), HANGZHOU ALLTEST BIOTECH CO. LTD, and 3 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.