CORONAVIRUS - ANVISA Registration 80680420058

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 80680420058 and manufactured by manufacturer not specified. The registration is held by BIO BRASIL BIOTECNOLOGIA LTDA with validity until Jan 10, 2032.

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 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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80680420058
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Registration Details
ANVISA Registration Number: 80680420058
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

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

Registration Details

80680420058

25351130679202225

10942372000190

Company Information

Dates and Status

Aug 01, 2022

10/01/2032

09/18/2025 19:00:01

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

Registration Details

80680420058

25351130679202225

10942372000190

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 01, 2022

10/01/2032

09/18/2025 19:00:01