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CORONAVIRUS - ANVISA Registration 82036180017

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 82036180017 and manufactured by manufacturer not specified. The registration is held by CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDA 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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82036180017
2 Related Devices
Registration Details
ANVISA Registration Number: 82036180017
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Related Devices (2)

Corona Virus (COVID-19) Antigen Rapid Test (Colloidal Gold)
Risk Class III

Registration Details

82036180017

25351319859202173

37026700000165

Dates and Status

Nov 16, 2021

16/11/2031

09/18/2025 19:00:01

Corona Virus (COVID-19) Antigen Rapid Test (Colloidal Gold)
Risk Class III

Registration Details

82036180017

25351319859202173

37026700000165

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 16, 2021

16/11/2031

09/18/2025 19:00:01