CORONAVIRUS - ANVISA Registration 80464810762

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 80464810762 and manufactured by manufacturer not specified. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until Apr 05, 2031.

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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80464810762
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Registration Details
ANVISA Registration Number: 80464810762
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Quick Profile SARS-CoV-2 RBD Antibody Test
Risk Class III

Registration Details

80464810762

25351954021202121

09377976000152

Dates and Status

Apr 05, 2021

05/04/2031

09/18/2025 19:00:01

Quick Profile SARS-CoV-2 RBD Antibody Test
Risk Class III

Registration Details

80464810762

25351954021202121

09377976000152

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 05, 2021

05/04/2031

09/18/2025 19:00:01