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COMBINED PARAMETERS - RESPIRATORY PANEL - ANVISA Registration 80680420057

Access comprehensive regulatory information for COMBINED PARAMETERS - RESPIRATORY PANEL in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80680420057 and manufactured by manufacturer not specified. The registration is held by BIO BRASIL BIOTECNOLOGIA LTDA with validity until Dec 06, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including CERTEST BIOTEC, S.L., ROCHE MOLECULAR SYSTEMS, INC, 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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80680420057
2 Related Devices
Registration Details
ANVISA Registration Number: 80680420057
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Related Devices (2)

Veri-Q COVID-19 & Influenza A/B Kit de Detecção Multiplex (CoVFLU-VM)
Risk Class III

Registration Details

80680420057

25351130609202277

10942372000190

Company Information

Dates and Status

Aug 01, 2022

06/12/2031

09/18/2025 19:00:01

Veri-Q COVID-19 & Influenza A/B Kit de Detecção Multiplex (CoVFLU-VM)
Risk Class III

Registration Details

80680420057

25351130609202277

10942372000190

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 01, 2022

06/12/2031

09/18/2025 19:00:01