ANVISA registration 81086830105ActiveSELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)
ANVISA Registration Number: 81086830105FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDAVEDALABRisk Class II
Device names
- Technical name
- SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)
- Risk class
- Class II
PT: AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)
Registration details
- Registration Number
- 81086830105
- Process Number
- 25351140680202519
- CNPJ
- 20037992000139
Company information
- Registration Holder
- FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA
- Manufacturer
- VEDALAB
- Manufacturing Country
- France
PT: FRANÇA
Dates and status
- Publication Date
- Sep 15, 2025
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81086830105 and manufactured by VEDALAB. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).
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