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CORONAVIRUS - ANVISA Registration 10230730179

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 10230730179 and manufactured by VIRAMED BIOTECH AG.. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until May 08, 2033.

This page provides complete technical specifications for 2 related devices, 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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10230730179
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Registration Details
ANVISA Registration Number: 10230730179
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Related Devices (2)

SARS-CoV-2 NT Chip Test Kit
Risk Class III

Registration Details

10230730179

25351028102202335

52541273000147

Company Information

Germany
PT: ALEMANHA

Dates and Status

May 08, 2023

08/05/2033

09/18/2025 19:00:01

SARS-CoV-2 NT Chip Test Kit
Risk Class III

Registration Details

10230730179

25351028102202335

52541273000147

Company Information

Dates and Status

May 08, 2023

08/05/2033

09/18/2025 19:00:01