Anuscope - ANVISA Registration 81464750007

Access comprehensive regulatory information for Anuscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81464750007 and manufactured by SUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTD. The registration is held by Domo Salute Consultoria Regulatória 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 KOLPLAST CI LTDA, HEXAGON INDUSTRIA E COMÉRCIO DE IMPLANTES ORTOPÉDICOS 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.