CORONAVIRUS - ANVISA Registration 80464810788

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 80464810788 and manufactured by LUMIQUICK DIAGNOSTICS. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until Feb 21, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

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80464810788
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Registration Details
ANVISA Registration Number: 80464810788
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

QuickPROFILE COVID-19 Antigen Test Card
Risk Class III

Registration Details

80464810788

25351021124202293

09377976000152

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 21, 2022

21/02/2032

09/18/2025 19:00:01

QuickPROFILE COVID-19 Antigen Test Card
Risk Class III

Registration Details

80464810788

25351021124202293

09377976000152

Dates and Status

Feb 21, 2022

21/02/2032

09/18/2025 19:00:01