ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.·Registered August 12, 2019ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT EL EQUIPO DE CONTROLES ALINITY C FERRITIN/MYOGLOBIN/IGE SE UTILIZA PARA LA MONITORIZACIÓN DEL CONTROL DE CALIDAD DE LOS RESULTADOS OBTENIDOS CON EL ENSAYO ALINITY C MYOGLOBIN POR TURBIMETRÍA.
ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT THE ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT IS USED FOR QUALITY CONTROL MONITORING OF THE RESULTS OBTAINED WITH THE ALINITY C MYOGLOBIN TEST BY TURBIMETRY.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO CONTROL
- Trade Name (English)
- REACTIVE CONTROL
- Analysis ID
- 1594R2019 SSA
- Registration Date
- August 12, 2019
- Name (Spanish)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT (ALINITY C FERRITIN/MYOGLOBIN/IGE CONTROL KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1594R2019 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on August 12, 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.