ALINITY C AMMONIA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MEXICO SA DE CV·Registered January 23, 2019ENSAYO PARA LA DETERMINACION ENZIMATICA DE AMONIO
TEST FOR THE ENZYMATIC DETERMINATION OF AMMONIUM
- 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 DETERMINACION ENZIMATICA DE AMONIO
- Trade Name (English)
- TEST FOR THE ENZYMATIC DETERMINATION OF AMMONIUM
- Analysis ID
- 50R2019 SSA
- Registration Date
- January 23, 2019
- Name (Spanish)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
- Name (English)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
Access comprehensive regulatory information for ALINITY C AMMONIA (ALINITY C 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 50R2019 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 23, 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.