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ANVISA registration 10208250058Active

SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)

ANVISA Registration Number: 10208250058DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDABEIJING CORE TECHNOLOGY 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
ANDALAN DIAGNÓSTICOS - TESTE DE GRAVIDEZ
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Risk class
Class II
Registration details
Registration Number
10208250058
Process Number
25351521897202356
CNPJ
38756680000140
Company information
Registration Holder
DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA
Manufacturer
BEIJING CORE TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Sep 04, 2023
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 10208250058 and manufactured by BEIJING CORE TECHNOLOGY CO., LTD.. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL 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.