ALINITY I CORTISOL
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MEXICO SA DE CV·Registered January 03, 2018ES UN INMUNOANALISIS DE MICROPARTICULAS (CMIA) UTILIZADO PARA LA DETERMINACION CUANTITATIVA DE CORTISOL EN SUERO, PLASMA U ORINA HUMANOS
IT IS A MICROPARTICLE IMMUNOASSAY (CMIA) USED FOR THE QUANTITATIVE DETERMINATION OF CORTISOL IN HUMAN SERUM, PLASMA OR 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 CORTISOL
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF CORTISOL
- Analysis ID
- 24R2018 SSA
- Registration Date
- January 03, 2018
- Name (Spanish)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
- Name (English)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
Access comprehensive regulatory information for ALINITY I CORTISOL (ALINITY I CORTISOL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 24R2018 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 03, 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.