AUTOCAL
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.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- AUTOCAL HA SIDO DISEÑADO PARA LACALIBRACIÓN DE LOS MÉTODOS DEANÁLISIS DE HUMAN EN LOSANALIZADORES
- Trade Name (English)
- AUTOCAL HAS BEEN DESIGNED FOR THE CALIBRATION OF HUMAN ANALYSIS METHODS IN ANALYZERS
- Analysis ID
- 1440R2021 SSA
- Registration Date
- September 20, 2021
- Name (Spanish)
- DICIPA, S.A. DE C.V.
- Name (English)
- DICIPA, S.A. DE C.V.
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.