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ANVISA registration 80524900023Active

SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)

ANVISA Registration Number: 80524900023BIO ADVANCE DIAGNOSTICOS LTDASHANGHAI SINOVAE TECH CO. LTD.Risk Class II
Verified
Device names
Technical name
SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)
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PT: AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)
Commercial name
Teste Rápido de Gravidez por hCG (10 mlU/mL)
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Risk class
Class II
Registration details
Registration Number
80524900023
Process Number
25351535961201465
CNPJ
09593438000103
Company information
Registration Holder
BIO ADVANCE DIAGNOSTICOS LTDA
Manufacturer
SHANGHAI SINOVAE TECH CO. LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 12, 2015
Status
Active
Official value: VIGENTE
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 80524900023 and manufactured by SHANGHAI SINOVAE TECH CO. LTD.. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).

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.