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CORONAVIRUS - ANVISA Registration 80332010057

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 80332010057 and manufactured by manufacturer not specified. The registration is held by LB DIAGNÓSTICA COMERCIO DE PRODUTOS MÉDICOS HOSPITALARES LTDA epp with validity until Aug 06, 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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80332010057
2 Related Devices
Registration Details
ANVISA Registration Number: 80332010057
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Related Devices (2)

SARS-CoV-2 ViraChip® IgG Control
Risk Class III

Registration Details

80332010057

25351712310202073

07668811000104

Dates and Status

Aug 06, 2020

06/08/2030

09/18/2025 19:00:01

SARS-CoV-2 ViraChip® IgG Control
Risk Class III

Registration Details

80332010057

25351712310202073

07668811000104

Company Information

Germany
PT: ALEMANHA

Dates and Status

Aug 06, 2020

06/08/2030

09/18/2025 19:00:01