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CALIBRADOR HUMANO BIOSYSTEMS, BIOSIMEX - COFEPRIS Registration 1856R2019 SSA

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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COFEPRIS Official Data
Clase I
1856R2019 SSA
CALIBRADOR HUMANO BIOSYSTEMS, BIOSIMEX
COFEPRIS Analysis ID: 1856R2019 SSA
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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 DIAGNร“STICO
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 (English)
BIO SIMEX, S.A. DE C.V.