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CORONAVIRUS - ANVISA Registration 80926150051

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 80926150051 and manufactured by manufacturer not specified. The registration is held by ALPHALIFE MATERIAIS MÉDICO HOSPITALARES LTDA. with validity until Dec 28, 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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80926150051
2 Related Devices
Registration Details
ANVISA Registration Number: 80926150051
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Related Devices (2)

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

Registration Details

80926150051

25351532075202058

12456120000187

Company Information

Dates and Status

Dec 28, 2020

28/12/2030

09/18/2025 19:00:01

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

Registration Details

80926150051

25351532075202058

12456120000187

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Dec 28, 2020

28/12/2030

09/18/2025 19:00:01