CORONAVIRUS - ANVISA Registration 80537410079

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 80537410079 and manufactured by CELER BIOTECNOLOGIA S/A. The registration is held by CELER BIOTECNOLOGIA S/A with validity until Nov 12, 2030.

This page provides complete technical specifications for this device, 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.