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CORONAVIRUS - ANVISA Registration 80583710055

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 80583710055 and manufactured by HI TECHNOLOGIES LTDA. The registration is held by HI TECHNOLOGIES LTDA with validity until Feb 03, 2035.

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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80583710055
Registration Details
ANVISA Registration Number: 80583710055
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Device Details

Flow COVID Ag
Risk Class III

Registration Details

80583710055

25351196789202411

07111023000112

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 03, 2025

03/02/2035

09/18/2025 19:00:01