CORONAVIRUS - ANVISA Registration 80113770026

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 80113770026 and manufactured by GUANGZHOU WONDFO BIOTECH CO.LTD. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP with validity until Mar 08, 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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80113770026
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Registration Details
ANVISA Registration Number: 80113770026
Janaina dos Santos de Miranda

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Related Devices (2)

Família Teste n-CoV19 Antígeno
Risk Class III

Registration Details

80113770026

25351960128202116

03098281000155

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 08, 2021

08/03/2031

09/18/2025 19:00:01

Família Teste n-CoV19 Antígeno
Risk Class III

Registration Details

80113770026

25351960128202116

03098281000155

Company Information

Dates and Status

Mar 08, 2021

08/03/2031

09/18/2025 19:00:01