Specula - ANVISA Registration 10237610168

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 10237610168 and manufactured by KOLPLAST CI LTDA. The registration is held by KOLPLAST CI 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 PROFESSIONAL HOSPITAL FURNISHERS, BAUSCH & LOMB 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.