DENGUE - ANVISA Registration 82444370171

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 82444370171 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by Enzytec Biotecnologia Ltda. with validity until Jan 06, 2035.

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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82444370171
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Registration Details
ANVISA Registration Number: 82444370171
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Dengue NS1 Ag Plus Rapid Test Cassette (Whole Blood/Serum/Plasma)
Risk Class III

Registration Details

82444370171

25351370073202492

07214566000165

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 06, 2025

06/01/2035

09/18/2025 19:00:01

Dengue NS1 Ag Plus Rapid Test Cassette (Whole Blood/Serum/Plasma)
Risk Class III

Registration Details

82444370171

25351370073202492

07214566000165

Company Information

Dates and Status

Jan 06, 2025

06/01/2035

09/18/2025 19:00:01