DENGUE - ANVISA Registration 82195300011

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82195300011 and manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA with validity until Dec 02, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Eco Diagnostica Ltda, HANGZHOU ALLTEST BIOTECH CO. LTD, 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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82195300011
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Registration Details
ANVISA Registration Number: 82195300011
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

VivaDiag Dengue IgG/IgM and NS1 Combo Rapid Test
Risk Class III

Registration Details

82195300011

25351309164202426

27939884000109

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Dec 02, 2024

02/12/2034

09/18/2025 19:00:01

VivaDiag Dengue IgG/IgM and NS1 Combo Rapid Test
Risk Class III

Registration Details

82195300011

25351309164202426

27939884000109

Company Information

Dates and Status

Dec 02, 2024

02/12/2034

09/18/2025 19:00:01