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EMIT II PLUS 6-ACETYLMORPHINE ASSAY - COFEPRIS Registration 679R2018 SSA

Access comprehensive regulatory information for EMIT II PLUS 6-ACETYLMORPHINE ASSAY (EMIT II PLUS 6-ACETYLMORPHINE ASSAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 679R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 07, 2018.

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
679R2018 SSA
EMIT II PLUS 6-ACETYLMORPHINE ASSAY
COFEPRIS Analysis ID: 679R2018 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DE 6-ACETILMORFINA

English

REAGENT FOR THE DETERMINATION OF 6-ACETHYLMORPHINE

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 PARA LA DETERMINACION DE 6-ACETILMORFINA
Trade Name (English)
REAGENT FOR THE DETERMINATION OF 6-ACETHYLMORPHINE
Registration Information
Analysis ID
679R2018 SSA
Registration Date
March 07, 2018
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR