Pure Global AI
ANVISA registration 82195300015Active

SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH)

ANVISA Registration Number: 82195300015PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDASEJOY BIOMEDICAL CO., LTD.Risk Class II
Verified
Device names
Technical name
SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH)
View exact technical-name matches →
PT: AUTOTESTE PARA HORMÔNIO FOLÍCULO ESTIMULANTE (FSH)
Commercial name
Teste de Menopausa FSH em uma etapa
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
82195300015
Process Number
25351052303202515
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
SEJOY BIOMEDICAL CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 05, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82195300015 and manufactured by SEJOY BIOMEDICAL 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.