CORONAVIRUS - ANVISA Registration 80638720175

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 80638720175 and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until May 03, 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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80638720175
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Registration Details
ANVISA Registration Number: 80638720175
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

COVID-19 RBD RAPID TEST
Risk Class III

Registration Details

80638720175

25351040876202172

11462456000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 03, 2021

03/05/2031

09/18/2025 19:00:01

COVID-19 RBD RAPID TEST
Risk Class III

Registration Details

80638720175

25351040876202172

11462456000190

Company Information

Dates and Status

May 03, 2021

03/05/2031

09/18/2025 19:00:01