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CORONAVIRUS - ANVISA Registration 81472060032

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 81472060032 and manufactured by ADVAGEN BIOTECH LTDA. The registration is held by ADVAGEN BIOTECH LTDA with validity until Mar 22, 2031.

This page provides complete technical specifications for this device, regulatory compliance details, 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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81472060032
Registration Details
ANVISA Registration Number: 81472060032
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Device Details

ADVA Covid-19 RT-LAMP
Risk Class III

Registration Details

81472060032

25351093451202166

22565307000172

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 22, 2021

22/03/2031

09/18/2025 19:00:01