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ANVISA registration 82195300012Active

FERTILITY SELF-TEST

ANVISA Registration Number: 82195300012PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDAACMEX BIO-TECHNOLOGY (CHONGQING) CO., LTD.Risk Class II
Verified
Device names
Technical name
FERTILITY SELF-TEST
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PT: AUTOTESTE PARA FERTILIDADE
Commercial name
Teste rápido de ovulação (LH)
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Risk class
Class II
Registration details
Registration Number
82195300012
Process Number
25351423602202468
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
ACMEX BIO-TECHNOLOGY (CHONGQING) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 13, 2025
Status
Active
Official value: VIGENTE
Last Updated
08/19/2026 19:00:01
About this record

Access comprehensive regulatory information for FERTILITY SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82195300012 and manufactured by ACMEX BIO-TECHNOLOGY (CHONGQING) CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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.