STREPTOCOCCUS - ANVISA Registration 80254180478

Access comprehensive regulatory information for STREPTOCOCCUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180478 and manufactured by manufacturer not specified. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Mar 17, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VEDALAB, Eco Diagnostica 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.