ROCHECARDIACPOCTROPONINTCONTROL - COFEPRIS Registration 1396R2020 SSA
Access comprehensive regulatory information for ROCHECARDIACPOCTROPONINTCONTROL (ROCHECARDIACPOCTROPONINTCONTROL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1396R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on October 12, 2020.
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.
ROCHE CARDIAC POC TROPONIN T CONTROLESTÁDESTINADOALCONTROLDECALIDADDELAPRUEBAROCHECARDIACPOCTROPONINTEMPLEANDO LOS ANALIZADORES ROCHE.AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARA USO EXCLUSIVO EN LABORATORIOSCLÍNICOS O DE GABINETES.
ROCHE CARDIAC POC TROPONIN T CONTROL IS INTENDED FOR QUALITY CONTROL OF THE ROCHECARDIACPOCTROPONINT TEST USING ROCHE ANALYSERS. DIAGNOSTICAGENTFORUSEINVITRO. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.