RUBELLA VIRUS - ANVISA Registration 81325990332

Access comprehensive regulatory information for RUBELLA VIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81325990332 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Feb 14, 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 ROCHE DIAGNOSTICS GMBH, ABBOTT IRELAND DIAGNOSTIC DIVISION, 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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81325990332
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Registration Details
ANVISA Registration Number: 81325990332
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Teste de Anticorpos Rubéola IgG/IgM (Sangue Total/Soro/Plasma)
Risk Class III

Registration Details

81325990332

25351512324202331

19933144000129

Dates and Status

Feb 14, 2024

14/02/2034

09/18/2025 19:00:01

Família Teste de Anticorpos Rubéola IgG/IgM (Sangue Total/Soro/Plasma)
Risk Class III

Registration Details

81325990332

25351512324202331

19933144000129

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 14, 2024

14/02/2034

09/18/2025 19:00:01