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MULTIGENT BENZODIAZEPINES REAGENT KIT - COFEPRIS Registration 2193R2019 SSA

Access comprehensive regulatory information for MULTIGENT BENZODIAZEPINES REAGENT KIT (MULTIGENT BENZODIAZEPINES REAGENT 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 2193R2019 SSA and manufactured by ABBOTT LABORATORIES DE Mร‰XICO, S.A. DE C.V.. The device was registered on November 27, 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
2193R2019 SSA
MULTIGENT BENZODIAZEPINES REAGENT KIT
COFEPRIS Analysis ID: 2193R2019 SSA
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Product Use / Uso del Producto
Spanish

EL ENSAYO MULTIGENT BENZODIAZEPINES SE UTILIZA PARA LA DETERMINACIร“N CUALITATIVA Y SEMICUANTITATIVA DE LA BENZODIACEPINA EN ORINA HUMANA CON LOS ARCHITECT CSYSTEMS. AGENTE DE DIAGNร“S

English

THE MULTIGENT BENZODIAZEPINES ASSAY IS USED FOR THE QUALITATIVE AND SEMIQUANTITATIVE DETERMINATION OF BENZODIAZEPINE IN HUMAN URINE WITH ARCHITECT CSYSTEMS. DIAGNOSTIC AGENT

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)
REACTIVOS PARA LA DETERMINACIร“N DE LA BENZODIACEPINA EN ORINA HUMANA.
Trade Name (English)
REAGENTS FOR THE DETERMINATION OF BENZODIAZEPINE IN HUMAN URINE.
Registration Information
Analysis ID
2193R2019 SSA
Registration Date
November 27, 2019
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE Mร‰XICO, S.A. DE C.V.