INFLUENZA VIRUS A and B - ANVISA Registration 80524900040

Access comprehensive regulatory information for INFLUENZA VIRUS A and B in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80524900040 and manufactured by CTK BIOTECH, INC.. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Aug 15, 2026.

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 KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA, 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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80524900040
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Registration Details
ANVISA Registration Number: 80524900040
Janaina dos Santos de Miranda

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Related Devices (2)

TESTE RÁPIDO ONSITE INFLUENZA A/B
Risk Class III

Registration Details

80524900040

25351938434201600

09593438000103

Company Information

CTK BIOTECH, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 15, 2016

15/08/2026

09/18/2025 19:00:01

TESTE RÁPIDO ONSITE INFLUENZA A/B
Risk Class III

Registration Details

80524900040

25351938434201600

09593438000103

Company Information

Dates and Status

Aug 15, 2016

15/08/2026

09/18/2025 19:00:01