DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN
LOS MÉTODOS HCG Y LHCG ESTÁN DISEÑADOS PARA LA DETERMINACIÓN CUANTITATIVA DE LA GONADOTROPINA CORIÓNICA HUMANA INTACTA EN PLASMA Y SUERO HUMANOS
THE HCG AND LHCG METHODS ARE DESIGNED FOR THE QUANTITATIVE DETERMINATION OF INTACT HUMAN CHORIONIC GONADOTROPIN IN HUMAN PLASMA AND SERUM
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA LA DETERMINACIÓN DE GONADOTROPINA CORIÓNICA HUMANA
- Trade Name (English)
- ASSAY FOR THE DETERMINATION OF HUMAN CHORIONIC GONADOTROPIN
- Analysis ID
- 544R2019 SSA
- Registration Date
- March 14, 2019
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
Access comprehensive regulatory information for DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN (DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 544R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on March 14, 2019.
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.