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ASCOT INSTRUMENTAL - COFEPRIS Registration 1594E2018 SSA

Access comprehensive regulatory information for ASCOT INSTRUMENTAL (ASCOT INSTRUMENTAL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1594E2018 SSA and manufactured by TRAUMASERVICE INTERNACIONAL, S.A. DE C.V.. The device was registered on June 19, 2018.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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
1594E2018 SSA
ASCOT INSTRUMENTAL
COFEPRIS Analysis ID: 1594E2018 SSA
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Product Use / Uso del Producto
Spanish

INSTRUMENTAL PARA EL SISTEMA ASCOT QUE SIRVE PARA LA ESTABILIZACIร“N VENTRAL DEL SEGMENTO CERVICAL C2-C7.

English

INSTRUMENTATION FOR THE ASCOT SYSTEM USED FOR VENTRAL STABILIZATION OF THE CERVICAL SEGMENT C2-C7.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
INSTRUMENTAL QUIRรšRGICO PARA LA ESTABILIZACIร“N VENTRAL DEL SEGMENTO CERVICAL
Trade Name (English)
SURGICAL INSTRUMENTS FOR VENTRAL STABILIZATION OF THE CERVICAL SEGMENT
Registration Information
Analysis ID
1594E2018 SSA
Registration Date
June 19, 2018
Manufacturer / Fabricante
Name (English)
TRAUMASERVICE INTERNACIONAL, S.A. DE C.V.