ZIKA - ANVISA Registration 81325990334

Access comprehensive regulatory information for ZIKA in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81325990334 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Feb 26, 2034.

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 Eco Diagnostica Ltda, VIRCELL S.L., 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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81325990334
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Registration Details
ANVISA Registration Number: 81325990334
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Teste de Combo Zika IgG/IgM e NS1 (sangue total/soro/plasma)
Risk Class IV

Registration Details

81325990334

25351511450202379

19933144000129

Dates and Status

Feb 26, 2024

26/02/2034

09/18/2025 19:00:01

Família Teste de Combo Zika IgG/IgM e NS1 (sangue total/soro/plasma)
Risk Class IV

Registration Details

81325990334

25351511450202379

19933144000129

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 26, 2024

26/02/2034

09/18/2025 19:00:01