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CORONAVIRUS - ANVISA Registration 80859840202

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 80859840202 and manufactured by SHANGAI BIOGERM MEDICAL TECHNOLOGY., LTD. LOCALIZADA. The registration is held by CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA. with validity until Apr 27, 2030.

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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80859840202
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Registration Details
ANVISA Registration Number: 80859840202
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Related Devices (2)

Novel Coronavirus (2019-nCoV) Nucleic Acid Detection Kit PCR-Fluorescence Probing
Risk Class III

Registration Details

80859840202

25351223955202036

13532259000125

Company Information

Dates and Status

Apr 27, 2020

27/04/2030

09/18/2025 19:00:01

Novel Coronavirus (2019-nCoV) Nucleic Acid Detection Kit PCR-Fluorescence Probing
Risk Class III

Registration Details

80859840202

25351223955202036

13532259000125

Dates and Status

Apr 27, 2020

27/04/2030

09/18/2025 19:00:01