SELF-TEST FOR SARS-COV-2 ANTIGEN (CORONAVIRUS) - ANVISA Registration 81403780003

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 81403780003 and manufactured by BEIJING LEPU MEDICAL TECHNOLOGY CO., LTD. The registration is held by ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDA with validity until Mar 21, 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, GENRUI BIOTECH INC., 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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81403780003
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Registration Details
ANVISA Registration Number: 81403780003
Janaina dos Santos de Miranda

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Related Devices (2)

Kit de Teste Rápido para Autoteste de Deteção de Antigénio do vírus SARS-CoV-2
Risk Class III

Registration Details

81403780003

25351052642202259

23241814000113

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 21, 2022

21/03/2032

09/18/2025 19:00:01

Kit de Teste Rápido para Autoteste de Deteção de Antigénio do vírus SARS-CoV-2
Risk Class III

Registration Details

81403780003

25351052642202259

23241814000113

Dates and Status

Mar 21, 2022

21/03/2032

09/18/2025 19:00:01