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INFLUENZA VIRUS A and B - ANVISA Registration 81472060049

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 81472060049 and manufactured by HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.. The registration is held by ADVAGEN BIOTECH LTDA with validity until Aug 25, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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81472060049
2 Related Devices
Registration Details
ANVISA Registration Number: 81472060049
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Related Devices (2)

Teste Rápido Influenza A + B
Risk Class III

Registration Details

81472060049

25351070972202579

22565307000172

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 25, 2025

25/08/2035

09/18/2025 19:00:01

Teste Rápido Influenza A + B
Risk Class III

Registration Details

81472060049

25351070972202579

22565307000172

Company Information

Dates and Status

Aug 25, 2025

25/08/2035

09/18/2025 19:00:01