KIT PARA LA DETERMINACIÓN DE SUBUNIDAD BETA LIBRE DE LA GONADOTROPINA CORIÓNICA HUMANA
Mexico·Clase II·III. Agentes de
diagnóstico·SIEMENS HEALTHCARE
DIAGNOSTICS, S. DE R.L. DE
C.V.·Registered March 20, 2024- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- ATELLICA IM FREE BETA HUMAN CHORIONIC GONADOTROPIN (FBHCG)
- Trade Name (English)
- ATELLICA IM FREE BETA HUMAN CHORIONIC GONADOTROPIN (FBHCG)
- Analysis ID
- 0756R2024 SSA
- Registration Date
- March 20, 2024
- 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 KIT PARA LA DETERMINACIÓN DE SUBUNIDAD BETA LIBRE DE LA GONADOTROPINA CORIÓNICA HUMANA (KIT PARA LA DETERMINACIÓN DE SUBUNIDAD BETA LIBRE DE LA GONADOTROPINA CORIÓNICA HUMANA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0756R2024 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on March 20, 2024.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.