CORONAVIRUS - ANVISA Registration 81268670004

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 81268670004 and manufactured by LUMIQUICK DIAGNOSTICS, INC.. The registration is held by ONEWAY IMPORTADORA E DISTRIBUIDORA LTDA with validity until Apr 16, 2030.

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.