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CORONAVIRUS - ANVISA Registration 81325990193

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 81325990193 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Sep 20, 2031.

This page provides complete technical specifications for 2 related devices, 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.

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81325990193
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Registration Details
ANVISA Registration Number: 81325990193
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Related Devices (2)

Cassete de Teste de Anticorpo IgG anti-S-RBD de Covid-19 ( Sangue total/Soro/ Plasma)
Risk Class III

Registration Details

81325990193

25351195837202110

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 20, 2021

20/09/2031

09/18/2025 19:00:01

Cassete de Teste de Anticorpo IgG anti-S-RBD de Covid-19 ( Sangue total/Soro/ Plasma)
Risk Class III

Registration Details

81325990193

25351195837202110

19933144000129

Dates and Status

Sep 20, 2021

20/09/2031

09/18/2025 19:00:01