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INFLUENZA VIRUS A and B - ANVISA Registration 10330660282

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 10330660282 and manufactured by manufacturer not specified. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Jan 20, 2030.

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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10330660282
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Registration Details
ANVISA Registration Number: 10330660282
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Related Devices (2)

Teste Rápido STANDARD Q Influenza A/B
Risk Class III

Registration Details

10330660282

25351012605202046

01057428000133

Company Information

Dates and Status

Jan 20, 2020

20/01/2030

09/18/2025 19:00:01

Teste Rápido STANDARD Q Influenza A/B
Risk Class III

Registration Details

10330660282

25351012605202046

01057428000133

Company Information

SD BIOSENSOR INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Jan 20, 2020

20/01/2030

09/18/2025 19:00:01