Specula - ANVISA Registration 81453610004

Access comprehensive regulatory information for Specula in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81453610004 and manufactured by ZUCK PAPEIS LTDA. The registration is held by ZUCK PAPEIS 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, 5 companies making the same product including PROFESSIONAL HOSPITAL FURNISHERS, KOLPLAST CI 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.