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CORONAVIRUS - ANVISA Registration 81464750072

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 81464750072 and manufactured by NANTONG EGENS BIOTECHNOLOGY CO., LTD.. The registration is held by Domo Salute Consultoria Regulatória Ltda with validity until Nov 12, 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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81464750072
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Registration Details
ANVISA Registration Number: 81464750072
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Related Devices (2)

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

Registration Details

81464750072

25351366078202097

26263959000103

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 12, 2020

12/11/2030

09/18/2025 19:00:01

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

Registration Details

81464750072

25351366078202097

26263959000103

Company Information

Dates and Status

Nov 12, 2020

12/11/2030

09/18/2025 19:00:01