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KIT PARA LA DETERMINACIÓN DE SUBUNIDAD BETA LIBRE DE LA GONADOTROPINA CORIÓNICA HUMANA - COFEPRIS Registration 0756R2024 SSA

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.

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COFEPRIS Official Data
Clase II
0756R2024 SSA
KIT PARA LA DETERMINACIÓN DE SUBUNIDAD BETA LIBRE DE LA GONADOTROPINA CORIÓNICA HUMANA
COFEPRIS Analysis ID: 0756R2024 SSA
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Device Classification
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)
Registration Information
Analysis ID
0756R2024 SSA
Registration Date
March 20, 2024
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.