Collection Vials - ANVISA Registration 81080249009

Access comprehensive regulatory information for Collection Vials in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81080249009 and manufactured by Plastimed do Brasil LTDA - ME. The registration is held by Plastimed do Brasil LTDA - ME 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 3P MEDICAL LTDA, SEROPLAST INDÚSTRIA E COMÉRCIO DE PRODUTOS HOSPITALARES LTDA -ME, 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.