ANVISA registration 81285200022Valid until Feb 10, 2035TREPONEMA PALLIDUM
ANVISA Registration Number: 81285200022FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMABEIJING HOTGEN BIOTECH CO., LTD.Risk Class IV
Device names
- Commercial name
- Teste Rápido de Anticorpos Totais Sífilis Bahiafarma (Ouro Coloidal)
- Risk class
- Class IV
Registration details
- Registration Number
- 81285200022
- Process Number
- 25351310011202421
- 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 TREPONEMA PALLIDUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81285200022 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.
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