ALINITY C IMMUNOGLOBULIN A
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.·Registered December 14, 2021ELENSAYOIMMUNOGLOBULINASEUTILIZAPARALADETERMINACIÓNCUANTITATIVADEIGAENSUEROOPLASMAHUMANOSENELALINITYCSYSTEM. AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVOENLABORATORIOS CLÍNICOS Y DE GABINETE.
The immunoglobulin assay is used for the quantitative determination of human serum or plasma in the alinitycsystem. DIAGNOSTICAGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL AND CABINET LABORATORIES.
- 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 DETERMINACIÓNCUANTITATIVA DE LA IGA.
- Trade Name (English)
- TEST FOR THE QUANTITATIVE DETERMINATION OF IGA.
- Analysis ID
- 2138R2021 SSA
- Registration Date
- December 14, 2021
- Name (Spanish)
- ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ALINITY C IMMUNOGLOBULIN A (ALINITY C IMMUNOGLOBULIN A) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2138R2021 SSA and manufactured by ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on December 14, 2021.
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.