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ANVISA registration 80074330069Active

AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)

ANVISA Registration Number: 80074330069GLOBO REAGENTES E EQUIPAMENTOS P/ LABORATORIOS LTDAQINGDAO HIGHTOP BIOTECH CO.,LTD.Risk Class II
Verified
Device names
Technical name
AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)
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Commercial name
Família Teste de Gravidez
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Risk class
Class II
Registration details
Registration Number
80074330069
Process Number
25351130409202648
CNPJ
02407183000190
Company information
Registration Holder
GLOBO REAGENTES E EQUIPAMENTOS P/ LABORATORIOS LTDA
Manufacturer
QINGDAO HIGHTOP BIOTECH CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Aug 17, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (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 80074330069 and manufactured by QINGDAO HIGHTOP BIOTECH CO.,LTD.. The registration is held by GLOBO REAGENTES E EQUIPAMENTOS P/ LABORATORIOS 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.