CORONAVIRUS - ANVISA Registration 80638720157

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 80638720157 and manufactured by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Aug 06, 2030.

This page provides complete technical specifications for this device, 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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80638720157
Registration Details
ANVISA Registration Number: 80638720157
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

COVID-19 COMBO RAPID TEST
Risk Class III

Registration Details

80638720157

25351536300202025

11462456000190

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 06, 2020

06/08/2030

09/18/2025 19:00:01