CORONAVIRUS - ANVISA Registration 80345000315

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 80345000315 and manufactured by manufacturer not specified. The registration is held by GOYAZES BIOTECNOLOGIA LTDA with validity until Aug 27, 2030.

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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80345000315
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Registration Details
ANVISA Registration Number: 80345000315
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FAMÍLIA VERI Q COVID-19 Kit de Detecção Multiplex nCoV-OM/nCoV-QM
Risk Class III

Registration Details

80345000315

25351536299202039

05658906000111

Company Information

Dates and Status

Aug 27, 2020

27/08/2030

09/18/2025 19:00:01

FAMÍLIA VERI Q COVID-19 Kit de Detecção Multiplex nCoV-OM/nCoV-QM
Risk Class III

Registration Details

80345000315

25351536299202039

05658906000111

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 27, 2020

27/08/2030

09/18/2025 19:00:01