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CORONAVIRUS - ANVISA Registration 80943610150

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 80943610150 and manufactured by manufacturer not specified. The registration is held by MINDRAY DO BRASIL COMÉRCIO E DISTRIBUIÇÃO DE EQUIPAMENTOS MÉDICOS LTDA. with validity until Oct 25, 2031.

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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80943610150
2 Related Devices
Registration Details
ANVISA Registration Number: 80943610150
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Related Devices (2)

Kit IgG S-RBD de SARS CoV-2 (CLIA)
Risk Class III

Registration Details

80943610150

25351195835202112

09058456000187

Dates and Status

Oct 25, 2021

25/10/2031

09/18/2025 19:00:01

Kit IgG S-RBD de SARS CoV-2 (CLIA)
Risk Class III

Registration Details

80943610150

25351195835202112

09058456000187

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 25, 2021

25/10/2031

09/18/2025 19:00:01