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ANVISA registration 80113770061Active

SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)

ANVISA Registration Number: 80113770061ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPPSEJOY BIOMEDICAL 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
Família Teste de Gravidez Digital com Indicador de Semanas
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Risk class
Class II
Registration details
Registration Number
80113770061
Process Number
25351203463202539
CNPJ
03098281000155
Company information
Registration Holder
ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP
Manufacturer
SEJOY BIOMEDICAL CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 12, 2026
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 80113770061 and manufactured by SEJOY BIOMEDICAL CO., LTD.. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP 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.