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CORONAVIRUS - ANVISA Registration 81733730016

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 81733730016 and manufactured by TRINITY BIOTECH PLC. The registration is held by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA with validity until Aug 14, 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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81733730016
2 Related Devices
Registration Details
ANVISA Registration Number: 81733730016
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Related Devices (2)

Uni-Gold™ CoV-2 Teste de antígeno
Risk Class III

Registration Details

81733730016

25351326887202228

15648426000204

Company Information

Ireland
PT: IRLANDA

Dates and Status

Aug 14, 2023

14/08/2033

09/18/2025 19:00:01

Uni-Gold™ CoV-2 Teste de antígeno
Risk Class III

Registration Details

81733730016

25351326887202228

15648426000204

Company Information

Dates and Status

Aug 14, 2023

14/08/2033

09/18/2025 19:00:01