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CORONAVIRUS - ANVISA Registration 81725630002

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 81725630002 and manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD.. The registration is held by MASTERS SPECIALITY PHARMA LTDA with validity until Sep 14, 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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81725630002
2 Related Devices
Registration Details
ANVISA Registration Number: 81725630002
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Related Devices (2)

Kit de Teste Covid 19(SARS-CoV-2) Anticorpo IgG/IgM Ouro Colidal
Risk Class III

Registration Details

81725630002

25351603789202058

14821008000123

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 14, 2020

14/09/2030

09/18/2025 19:00:01

Kit de Teste Covid 19(SARS-CoV-2) Anticorpo IgG/IgM Ouro Colidal
Risk Class III

Registration Details

81725630002

25351603789202058

14821008000123

Company Information

Dates and Status

Sep 14, 2020

14/09/2030

09/18/2025 19:00:01