ATELLICA CH AMONIACO
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered January 15, 2018PARA LA DETERMINACIÓN CUANTITATIVA DE AMONIACO EN SUERO, PLASMA Y ORINA HUMANOS
FOR THE QUANTITATIVE DETERMINATION OF AMMONIA IN HUMAN SERUM, PLASMA AND URINE
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA LA DETERMINACION DE AMONIACO
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF AMMONIA
- Analysis ID
- 183R2018 SSA
- Registration Date
- January 15, 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 AMONIACO (ATELLICA CH AMMONIA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 183R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on January 15, 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.