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CORONAVIRUS - ANVISA Registration 80102513011

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 80102513011 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until May 08, 2033.

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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80102513011
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Registration Details
ANVISA Registration Number: 80102513011
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Related Devices (2)

Kit teste de antígeno SARS-CoV-2 (ouro coloidal)
Risk Class III

Registration Details

80102513011

25351056767202339

04718143000194

Dates and Status

May 08, 2023

08/05/2033

09/18/2025 19:00:01

Kit teste de antígeno SARS-CoV-2 (ouro coloidal)
Risk Class III

Registration Details

80102513011

25351056767202339

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 08, 2023

08/05/2033

09/18/2025 19:00:01