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CORONAVIRUS - ANVISA Registration 81150720015

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 81150720015 and manufactured by SHANGHAI KEHUA BIO-ENGINEERING CO., LTD. The registration is held by BUZZY COMERCIAL IMPORTAÇÃO E EXPORTAÇÃO LTDA - ME with validity until Nov 16, 2031.

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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81150720015
2 Related Devices
Registration Details
ANVISA Registration Number: 81150720015
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Related Devices (2)

Kit de Diagnóstico para SARS-COV-2 IgM/IgG Anticorpos - Ouro Coloidal
Risk Class III

Registration Details

81150720015

25351467272202170

18980014000184

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 16, 2021

16/11/2031

09/18/2025 19:00:01

Kit de Diagnóstico para SARS-COV-2 IgM/IgG Anticorpos - Ouro Coloidal
Risk Class III

Registration Details

81150720015

25351467272202170

18980014000184

Company Information

Dates and Status

Nov 16, 2021

16/11/2031

09/18/2025 19:00:01