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ANVISA registration 81431270001Active

SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)

ANVISA Registration Number: 81431270001MEDIHOSP DISTRIBUIDORA DE MATERIAIS MEDICO HOSPITALAR - LTDA - MESEJOY 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
Teste de gravidez - Baby Tech Macrolife
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Risk class
Class II
Registration details
Registration Number
81431270001
Process Number
25351184459202564
CNPJ
22949063000121
Company information
Registration Holder
MEDIHOSP DISTRIBUIDORA DE MATERIAIS MEDICO HOSPITALAR - LTDA - ME
Manufacturer
SEJOY BIOMEDICAL CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Dec 01, 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 81431270001 and manufactured by SEJOY BIOMEDICAL CO., LTD.. The registration is held by MEDIHOSP DISTRIBUIDORA DE MATERIAIS MEDICO HOSPITALAR - LTDA - ME 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.