CORONAVIRUS - ANVISA Registration 81325990166

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 81325990166 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Mar 15, 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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81325990166
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Registration Details
ANVISA Registration Number: 81325990166
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Teste Rápido Ag Oral COVID-19
Risk Class III

Registration Details

81325990166

25351874415202104

19933144000129

Dates and Status

Mar 15, 2021

15/03/2031

09/18/2025 19:00:01

Família Teste Rápido Ag Oral COVID-19
Risk Class III

Registration Details

81325990166

25351874415202104

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 15, 2021

15/03/2031

09/18/2025 19:00:01