CORONAVIRUS - ANVISA Registration 80113770027

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 80113770027 and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP with validity until Jun 14, 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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80113770027
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Registration Details
ANVISA Registration Number: 80113770027
Janaina dos Santos de Miranda

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Related Devices (2)

FAMILIA TESTE COVID-19 SALIVA
Risk Class III

Registration Details

80113770027

25351564709202112

03098281000155

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 14, 2021

14/06/2031

09/18/2025 19:00:01

FAMILIA TESTE COVID-19 SALIVA
Risk Class III

Registration Details

80113770027

25351564709202112

03098281000155

Company Information

Dates and Status

Jun 14, 2021

14/06/2031

09/18/2025 19:00:01