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CORONAVIRUS - ANVISA Registration 81403780002

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 81403780002 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 Nov 30, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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81403780002
2 Related Devices
Registration Details
ANVISA Registration Number: 81403780002
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Related Devices (2)

Kit de Teste Rápido com Antígeno de SARS-CoV-2
Risk Class III

Registration Details

81403780002

25351311166202051

23241814000113

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 30, 2020

30/11/2030

09/18/2025 19:00:01

Kit de Teste Rápido com Antígeno de SARS-CoV-2
Risk Class III

Registration Details

81403780002

25351311166202051

23241814000113

Dates and Status

Nov 30, 2020

30/11/2030

09/18/2025 19:00:01