SELF-TEST FOR SARS-COV-2 ANTIGEN (CORONAVIRUS) - ANVISA Registration 80207450028

Access comprehensive regulatory information for SELF-TEST FOR SARS-COV-2 ANTIGEN (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 80207450028 and manufactured by GENRUI BIOTECH INC.. The registration is held by 1000MEDIC DISTRIBUIDORA IMPORTADORA EXPORTADORA DE MEDICAMENTOS LTDA with validity until Aug 08, 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 HANGZHOU ALLTEST BIOTECH CO. LTD, ASSURE TECH. (HANGZHOU) CO., LTD., 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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80207450028
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Registration Details
ANVISA Registration Number: 80207450028
Janaina dos Santos de Miranda

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Related Devices (2)

Kit de Teste de antígeno SARS-CoV 2 (ouro coloidal)
Risk Class III

Registration Details

80207450028

25351162085202283

05993698000107

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 08, 2022

08/08/2032

09/18/2025 19:00:01

Kit de Teste de antígeno SARS-CoV 2 (ouro coloidal)
Risk Class III

Registration Details

80207450028

25351162085202283

05993698000107

Dates and Status

Aug 08, 2022

08/08/2032

09/18/2025 19:00:01