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ANVISA registration 81285200023Valid until Feb 10, 2035

DENGUE

ANVISA Registration Number: 81285200023FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMABEIJING HOTGEN BIOTECH CO., LTD.Risk Class III
Verified
Device names
Technical name
DENGUE
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Commercial name
Teste Rápido de Antígeno NS1 Dengue Bahiafarma (Ouro Coloidal)
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Risk class
Class III
Registration details
Registration Number
81285200023
Process Number
25351307277202497
CNPJ
13078518000190
Company information
Registration Holder
FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMA
Manufacturer
BEIJING HOTGEN BIOTECH CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Feb 10, 2025
Validity
10/02/2035
Last Updated
08/18/2026 19:00:00
About this record

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 shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.