CORONAVIRUS - ANVISA Registration 80927230008

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80927230008 and manufactured by manufacturer not specified. The registration is held by CONSUMERSLAB PRODUTOS PARA LABORATÓRIOS E HOSPITAIS LTDA. EPP with validity until Aug 12, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., 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.