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CORONAVIRUS - ANVISA Registration 80345000328

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80345000328 and manufactured by MICOBIOMED CO., LTD.. The registration is held by GOYAZES BIOTECNOLOGIA LTDA with validity until Jan 10, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., 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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80345000328
2 Related Devices
Registration Details
ANVISA Registration Number: 80345000328
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Related Devices (2)

Veri-Q COVID-19 Ag Rapid Test
Risk Class III

Registration Details

80345000328

25351881198202109

05658906000111

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jan 10, 2022

10/01/2032

09/18/2025 19:00:01

Veri-Q COVID-19 Ag Rapid Test
Risk Class III

Registration Details

80345000328

25351881198202109

05658906000111

Company Information

Dates and Status

Jan 10, 2022

10/01/2032

09/18/2025 19:00:01