Specula - ANVISA Registration 81861779004

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 81861779004 and manufactured by SILLMED INDUSTRIA E COMÉRCIO DE PRODUTOS EM SILICONE LTDA. The registration is held by SILLMED INDUSTRIA E COMÉRCIO DE PRODUTOS EM SILICONE 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, 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.