CORONAVIRUS - ANVISA Registration 82011140001

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 82011140001 and manufactured by manufacturer not specified. The registration is held by vertical distribuidora de medicamentos ltda. with validity until Aug 27, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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82011140001
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Registration Details
ANVISA Registration Number: 82011140001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Teste Rápido para COVID-19 Ouro Coloidal
Risk Class III

Registration Details

82011140001

25351494655202030

21774568000130

Company Information

Dates and Status

Aug 27, 2020

27/08/2030

09/18/2025 19:00:01

Teste Rápido para COVID-19 Ouro Coloidal
Risk Class III

Registration Details

82011140001

25351494655202030

21774568000130

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 27, 2020

27/08/2030

09/18/2025 19:00:01