LIAISON® SHBG
Mexico·Clase I·III. DIAGNOSTIC AGENTS·DIASORIN MÉXICO, S.A. DE C.V.·Registered June 19, 2018EL ENSAYO DIASORIN LIAISON® SHBG ES UN INMUNOENSAYO QUIMIOLUMINISCENTE (CLIA) IN VITRO INDICADO PARA LA DETERMINACIÓN CUANTITATIVA DE LA GLOBULINA FIJADORA DE HORMONAS SEXUALES EN SUERO Y PLASMA. EL ENSAYO LIAISON® SHBG ESTÁ INDICADO PARA SU USO COMO AYUD
THE DIASORIN LIAISON® SHBG ASSAY IS AN IN VITRO CHEMILUMINESCENT IMMUNOASSAY (CLIA) INDICATED FOR THE QUANTITATIVE DETERMINATION OF SERUM AND PLASMA SEX HORMONE BINDING GLOBULIN. THE LIAISON® SHBG ASSAY IS INDICATED FOR USE AS AN AID.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- KIT PARA LA DETERMINACIÓN DE LA GLOBULINA FIJADORA DE HORMONAS SEXUALES
- Trade Name (English)
- SEX HORMONE BINDING GLOBULIN DETERMINATION KIT
- Analysis ID
- 1582R2018 SSA
- Registration Date
- June 19, 2018
- Name (Spanish)
- DIASORIN MÉXICO, S.A. DE C.V.
- Name (English)
- DIASORIN MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for LIAISON® SHBG (LIAISON® SHBG) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1582R2018 SSA and manufactured by DIASORIN MÉXICO, S.A. DE C.V.. The device was registered on June 19, 2018.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.