CORONAVIRUS - ANVISA Registration 80049120108
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 80049120108 and manufactured by ALAMAR TECNO CIENTÍFICA LTDA. The registration is held by ALAMAR TECNO CIENTÍFICA LTDA with validity until Apr 30, 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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Registration Details
80049120108
25351212023202068
48044358000142
Company Information
Dates and Status
Apr 30, 2020
30/04/2030
09/18/2025 19:00:01
CORONAVIRUS
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Not specified
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Mar 19, 2020
CORONAVIRUS
CORONAVÍRUS RAPID TEST
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80638720148
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Not specified
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Not specified
81472060050
Aug 25, 2025
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81472060050
Aug 25, 2025
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Xpert Xpress CoV-2 plus
Not specified
81062710058
Aug 18, 2025