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NEPHSTAR C1 INACTIVADOR KIT - COFEPRIS Registration 1246R2020 SSA

Access comprehensive regulatory information for NEPHSTAR C1 INACTIVADOR KIT (NEPHSTAR C1 INACTIVADOR KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1246R2020 SSA and manufactured by KABLA COMERCIAL, S.A. DEC.V.. The device was registered on September 11, 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
1246R2020 SSA
NEPHSTAR C1 INACTIVADOR KIT
COFEPRIS Analysis ID: 1246R2020 SSA
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Product Use / Uso del Producto
Spanish

LA PRUEBA SE UTILIZA PARA LADETERMINACIร“N CUANTITATIVA DELINACTIVADOR C1 HUMANO EN SUERO COMOAYUDAENELDIAGNร“STICODELMETABOLISMOANORMAL DE C1IN

English

THE TEST IS USED FOR THE QUANTITATIVE DETERMINATION OF HUMAN C1 ACTIVATOR IN SERUM AS AN AID IN THE DIAGNOSIS OF NORMAL C1IN METABOLISM

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)
PRUEBA PARA LA DETERMINACIร“NDEL INACTIVADOR C1 (C1IN)
Trade Name (English)
TEST FOR THE DETERMINATION OF THE INACTIVATOR C1 (C1IN)
Registration Information
Analysis ID
1246R2020 SSA
Registration Date
September 11, 2020
Manufacturer / Fabricante
Name (English)
KABBALAH COMMERCIAL, S.A. DEC.V.