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IDYLLA™ MSI TEST - COFEPRIS Registration 0911R2022 SSA

Access comprehensive regulatory information for IDYLLA™ MSI TEST (IDYLLA™ MSI TEST) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0911R2022 SSA and manufactured by EMERGO,S.DER.L.DE C.V.. The device was registered on September 09, 2022.

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 II
0911R2022 SSA
IDYLLA™ MSI TEST
COFEPRIS Analysis ID: 0911R2022 SSA
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Product Use / Uso del Producto
Spanish

PARA LA DETECCIÓN CUALITATIVA DE UN PERFIL DE 7BIOMARCADORES MONOMÓRFICOS PARA LAIDENTIFICACIÓN DE CÁNCERES COLORRECTALES CONINESTABILIDAD DE MICROSATÉLITES (MSI).

English

FOR THE QUALITATIVE DETECTION OF A PROFILE OF 7 MONOMORPHIC BIOMARKERS FOR THE IDENTIFICATION OF COLORECTAL CANCERS WITH MICROSATELLITE INSTABILITY (MSI).

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
PRUEBAONCOLÓGICADEPCREN TIEMPO REAL.
Trade Name (English)
ONCOLOGY TESTTHEY ARE IN REAL TIME.
Registration Information
Analysis ID
0911R2022 SSA
Registration Date
September 09, 2022
Manufacturer / Fabricante
Name (English)
EMERGO,S.DER. L.DE C.V.