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CORONAVIRUS - ANVISA Registration 80859840219

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 80859840219 and manufactured by BIOSCIENCE (TIANJIN) DIAGNOSTIC TECHNOLOGY CO.,LTD. The registration is held by CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA. with validity until Aug 08, 2032.

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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80859840219
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Registration Details
ANVISA Registration Number: 80859840219
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Related Devices (2)

Novel Coronavirus (2019-nCoV) Neutralizing Antibody Rapid Test
Risk Class III

Registration Details

80859840219

25351239922202270

13532259000125

Company Information

Dates and Status

Aug 08, 2022

08/08/2032

09/18/2025 19:00:01

Novel Coronavirus (2019-nCoV) Neutralizing Antibody Rapid Test
Risk Class III

Registration Details

80859840219

25351239922202270

13532259000125

Dates and Status

Aug 08, 2022

08/08/2032

09/18/2025 19:00:01