Neurology Diagnostic Equipment - ANVISA Registration 10166369001

Access comprehensive regulatory information for Neurology Diagnostic Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10166369001 and manufactured by HP BIOPROTESES LTDA. The registration is held by HP BIOPROTESES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including HEMEDEX INC, and 4 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.