M-PIMA™ ANALYSER.
Mexico·Clase I·I. MEDICAL EQUIPMENT·ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.·Registered July 26, 2022ELM-PIMA™ANALYSERESUNANALIZADORDESOBREMESAAUTOMÁTICOYPORTÁTILPARAPROCESARCARTUCHOSDETESTM-PIMA™.ELM-PIMA™ANALYSERPUEDESERUSADOENLABORATORIOSYENENTORNOSEXTERNOS. PARAUSODIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO DELABORATORIOS CLÍNICOS Y DE GABINETE.
ELM-PIMA ANALYSERESUNDESKTOPANALYZERAUTOMATICAND PORTABLE FOR PROCESSING TESTM-PIMA CARTRIDGES.ELM-PIMA™™™ANALYSER CAN BE USED IN LABORATORIES AND EXTERNAL ENVIRONMENTS. FOR EXCLUSIVE USE OF CLINICAL AND CABINET LABORATORIES.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- ANALIZADOR DE SOBREMESAAUTOMÁTICOYPORTÁTILPARAPROCESAR CARTUCHOS DETEST M-PIMA™.
- Trade Name (English)
- AUTOMATIC AND PORTABLE BENCHTOP ANALYZER FOR PROCESSING M-PIMA™ TEST CARTRIDGES.
- Analysis ID
- 669E2022 SSA
- Registration Date
- July 26, 2022
- Name (Spanish)
- ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTTLABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for M-PIMA™ ANALYSER. (M-PIMA™ ANALYZE.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 669E2022 SSA and manufactured by ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on July 26, 2022.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.