CORONAVIRUS - ANVISA Registration 80502070102

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 80502070102 and manufactured by manufacturer not specified. The registration is held by MOBIUS LIFE SCIENCE INDUSTRIA E COMERCIO DE PRODUTOS PARA LABORATORIOS LTDA with validity until Nov 28, 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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80502070102
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Registration Details
ANVISA Registration Number: 80502070102
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Kit Master para Detecção do Coronavírus SARS-CoV-2 MRC
Risk Class III

Registration Details

80502070102

25351157568202266

04645160000149

Dates and Status

Nov 28, 2022

28/11/2032

09/18/2025 19:00:01

Família Kit Master para Detecção do Coronavírus SARS-CoV-2 MRC
Risk Class III

Registration Details

80502070102

25351157568202266

04645160000149

Company Information

VITRO SA
Spain
PT: ESPANHA

Dates and Status

Nov 28, 2022

28/11/2032

09/18/2025 19:00:01