CORONAVIRUS - ANVISA Registration 81325990122

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 81325990122 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Sep 17, 2030.

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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81325990122
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Registration Details
ANVISA Registration Number: 81325990122
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Tell Me Fast Teste para Detecção de Anticorpos IgG/IgM do Novo Coronavírus (COVID-19)
Risk Class III

Registration Details

81325990122

25351910386202062

19933144000129

Dates and Status

Sep 17, 2020

17/09/2030

09/18/2025 19:00:01

Família Tell Me Fast Teste para Detecção de Anticorpos IgG/IgM do Novo Coronavírus (COVID-19)
Risk Class III

Registration Details

81325990122

25351910386202062

19933144000129

Company Information

Canada
PT: CANADÁ

Dates and Status

Sep 17, 2020

17/09/2030

09/18/2025 19:00:01