Needle Phobia Device - ANVISA Registration 82113060001

Access comprehensive regulatory information for Needle Phobia Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82113060001 and manufactured by NOVO NORDISK A/S. The registration is held by NOVO NORDISK FARMACÊUTICA DO BRASIL 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 BIOMEDICAL EQUIPAMENTOS E PRODUTOS MÉDICO-CIRÚRGICOS LTDA., and 1 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.