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FLUID PACK 0018165300 - COFEPRIS Registration 1487R2020 SSA

Access comprehensive regulatory information for FLUID PACK 0018165300 (FLUID PACK 0018165300) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1487R2020 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on October 29, 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.

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COFEPRIS Official Data
Clase I
1487R2020 SSA
FLUID PACK 0018165300
COFEPRIS Analysis ID: 1487R2020 SSA
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Product Use / Uso del Producto
Spanish

FLUIDPACKSEUTILIZAPARALACALIBRACIร“NDE SODIO, POTASIO Y CLORURO UTILIZANDOLOS ANALIZADORES DE QUรMICA CLรNICA ILAB.

English

FLUIDPACK IS USED FOR SODIUM, POTASSIUM AND CHLORIDE CALIBRATION USING ILAB CLINICAL CHEMISTRY ANALYZERS.

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)
CALIBRADOR
Trade Name (English)
CALIBRADOR
Registration Information
Analysis ID
1487R2020 SSA
Registration Date
October 29, 2020
Manufacturer / Fabricante
Name (English)
I.L. DIAGNOSTICS, S.A. DE C.V.