CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 80120820010

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80120820010 and manufactured by manufacturer not specified. The registration is held by BIOLINE COMERCIAL LTDA with validity until Feb 20, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ABBOTT MEDICAL, COOK INCORPORATED, 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.