CORONAVIRUS - ANVISA Registration 80638720184

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 80638720184 and manufactured by manufacturer not specified. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Jun 28, 2031.

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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80638720184
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Registration Details
ANVISA Registration Number: 80638720184
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

COVID-19 RBD TEST CASSETE FIA
Risk Class III

Registration Details

80638720184

25351584584202147

11462456000190

Company Information

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01

COVID-19 RBD TEST CASSETE FIA
Risk Class III

Registration Details

80638720184

25351584584202147

11462456000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01