CORONAVIRUS - ANVISA Registration 81869080006

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 81869080006 and manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD.. The registration is held by SVAROG IMPORTACAO, EXPORTACAO E COMERCIO LTDA with validity until Jul 16, 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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81869080006
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Registration Details
ANVISA Registration Number: 81869080006
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Immupass VivaDiagTM SARS-CoV-2 IgM/IgG Rapid Test (COVID-19 IgM/IgG Rapid Test)
Risk Class III

Registration Details

81869080006

25351496382202068

08435221000102

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 16, 2020

16/07/2030

09/18/2025 19:00:01

Immupass VivaDiagTM SARS-CoV-2 IgM/IgG Rapid Test (COVID-19 IgM/IgG Rapid Test)
Risk Class III

Registration Details

81869080006

25351496382202068

08435221000102

Company Information

Dates and Status

Jul 16, 2020

16/07/2030

09/18/2025 19:00:01