AUTOCAL - COFEPRIS Registration 1440R2021 SSA
Access comprehensive regulatory information for AUTOCAL (AUTOCAL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1440R2021 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on September 20, 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.
AUTOCAL HA SIDO DISEÑADO PARA LACALIBRACIÓNDELOSMÉTODOSDEANÁLISISDE HUMAN EN LOS ANALIZADORES DEQUÍMICA CLÍNICA DE LAS SERIESAUTOHUMALYZERYHUMASTAR.AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVO EN LABORATORIOS CLÍNICOS ODE GABINETES.
AUTOCAL HAS BEEN DESIGNED FOR THE CALIBRATION OF HUMAN ANALYSIS METHODS IN THE CLINICAL CHEMISTRY ANALYZERS OF THE AUTOHUMALYZERAND HUMASTAR SERIES. DIAGNOSTICAGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL LABORATORIES OR CABINETS.