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DENGUE - ANVISA Registration 81285200023

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 81285200023 and manufactured by BEIJING HOTGEN BIOTECH CO., LTD. The registration is held by FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMA with validity until Feb 10, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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81285200023
2 Related Devices
Registration Details
ANVISA Registration Number: 81285200023
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Related Devices (2)

Teste Rápido de Antígeno NS1 Dengue Bahiafarma (Ouro Coloidal)
Risk Class III

Registration Details

81285200023

25351307277202497

13078518000190

Company Information

Dates and Status

Feb 10, 2025

10/02/2035

09/18/2025 19:00:01

Teste Rápido de Antígeno NS1 Dengue Bahiafarma (Ouro Coloidal)
Risk Class III

Registration Details

81285200023

25351307277202497

13078518000190

Dates and Status

Feb 10, 2025

10/02/2035

09/18/2025 19:00:01