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REACTIVO PARA DETERMINACIÓN DE OPIÁCEOS - COFEPRIS Registration 0495R2022 SSA

Access comprehensive regulatory information for REACTIVO PARA DETERMINACIÓN DE OPIÁCEOS (REACTIVO PARA DETERMINACIÓN DE OPIÁCEOS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0495R2022 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on June 16, 2022.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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
0495R2022 SSA
REACTIVO PARA DETERMINACIÓN DE OPIÁCEOS
COFEPRIS Analysis ID: 0495R2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
EMIT® II PLUS OPIATE ASSAY
Trade Name (English)
EMIT® II PLUS OPIATE ASSAY
Registration Information
Analysis ID
0495R2022 SSA
Registration Date
June 16, 2022
Manufacturer / Fabricante
Name (English)
BECKMAN COULTER DE MÉXICO, S.A. DE C.V.