ANVISA registration
Teste de Menopausa FSH em uma etapa
Registration 82195300015. AUTOTESTE PARA HORMÔNIO FOLÍCULO ESTIMULANTE (FSH)
Registration details
| Registration number | 82195300015 |
|---|---|
| Application number | 25351052303202515 |
| Technical name | AUTOTESTE PARA HORMÔNIO FOLÍCULO ESTIMULANTE (FSH) |
| Risk class | II |
| Published on | 05/05/2025 |
| Validity | Indefinite validity |
Registration holder
| Legal name | PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA |
|---|---|
| CNPJ | 27.939.884/0001-09 |
Manufacturer
- SEJOY BIOMEDICAL CO., LTD. CHINA, REPÚBLICA POPULAR
Other registrations held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDAview all
Sistema Digital de Teste de Ovulação LH
82195300004Sistema Digital de Teste de Gravidez - HCG
82195300005Sistema Digital de Teste de Menopausa FSH
82195300006VivaDiagTM hCG Pregnancy Rapid Test
82195300007CARTUCHO DE TESTE DO PAINEL DE LIPÍDIOS
82195300008Sistema de Monitoramento de Painel de Lipídios BF-101b
82195300009Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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