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INFLUENZA A VIRUS - ANVISA Registration 82149920029

Access comprehensive regulatory information for INFLUENZA A 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 82149920029 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA with validity until Jun 22, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including NOVATEC IMMUNDIAGNOSTICA GMBH TECHNOLOGIE & WALDPARK, R-BIOPHARM AG, 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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82149920029
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Registration Details
ANVISA Registration Number: 82149920029
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Related Devices (2)

Família VIASURE Flu Typing II Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920029

25351281418202353

35489323000175

Company Information

Spain
PT: ESPANHA

Dates and Status

Jun 12, 2023

22/06/2030

09/18/2025 19:00:01

Família VIASURE Flu Typing II Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920029

25351281418202353

35489323000175

Company Information

Dates and Status

Jun 12, 2023

22/06/2030

09/18/2025 19:00:01