ATELLICA CH C-REACTIVE PROTEIN_2 (CRP_2)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered March 06, 2018ENSAYO PARA LA DETRMINACION DE PROTEINA C-REACTIVA 2
ASSAY FOR THE DETRMINACION OF PROTEIN C-REACTIVE 2
- 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 DETRMINACION DE PROTEINA C-REACTIVA 2
- Trade Name (English)
- ASSAY FOR THE DETRMINACION OF PROTEIN C-REACTIVE 2
- Analysis ID
- 672R2018 SSA
- Registration Date
- March 06, 2018
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR
Access comprehensive regulatory information for ATELLICA CH C-REACTIVE PROTEIN_2 (CRP_2) (ATELLICA CH C-REACTIVE PROTEIN_2 (CRP_2)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 672R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 06, 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.