Mexico COFEPRIS registration 1856R2019 SSA

CALIBRADOR HUMANO BIOSYSTEMS, BIOSIMEX

EN: BIOSYSTEMS HUMAN CALIBRATOR, BIOSIMEX

Mexico·Clase I·III. DIAGNOSTIC AGENTS·BIO SIMEX, S.A. DE C.V.·Registered September 13, 2019

Product Use / Uso del Producto

Spanish

REACTIVO CALIBRADOR

English

CALIBRATOR REAGENT

Device classification

Risk Class / Clase de Riesgo: Clase I
Product Type (Spanish): III. AGENTES DE DIAGNÓSTICO
Product Type (English): III. DIAGNOSTIC AGENTS
Trade Name (Spanish): REACTIVO CALIBRADOR
Trade Name (English): CALIBRATOR REAGENT

Registration information

Analysis ID: 1856R2019 SSA
Registration Date: September 13, 2019

Manufacturer / Fabricante

Name (Spanish): BIO SIMEX, S.A. DE C.V.
Name (English): BIO SIMEX, S.A. DE C.V.

About this record

Access comprehensive regulatory information for CALIBRADOR HUMANO BIOSYSTEMS, BIOSIMEX (BIOSYSTEMS HUMAN CALIBRATOR, BIOSIMEX) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1856R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on September 13, 2019.

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.

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