CORONAVIRUS - ANVISA Registration 81285200019

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 81285200019 and manufactured by manufacturer not specified. The registration is held by FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMA with validity until Nov 25, 2034.

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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81285200019
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Registration Details
ANVISA Registration Number: 81285200019
Janaina dos Santos de Miranda

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Related Devices (2)

Teste de Antígeno do Novo Coronavírus 2019-nCoV Bahiafarma (Ouro Coloidal)
Risk Class III

Registration Details

81285200019

25351278461202412

13078518000190

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01

Teste de Antígeno do Novo Coronavírus 2019-nCoV Bahiafarma (Ouro Coloidal)
Risk Class III

Registration Details

81285200019

25351278461202412

13078518000190

Company Information

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01