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SISTEMA DE CIFOPLASTÍA SPASY MARCA SEAWON - COFEPRIS Registration 553E2019 SSA

Access comprehensive regulatory information for SISTEMA DE CIFOPLASTÍA SPASY MARCA SEAWON (SPASY KYPHOPLASTY SYSTEM SEAWON BRAND) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 553E2019 SSA and manufactured by TRAUMASERVICE INTERNACIONAL, S.A. DE C.V.. The device was registered on March 15, 2019.

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 II
553E2019 SSA
SISTEMA DE CIFOPLASTÍA SPASY MARCA SEAWON
COFEPRIS Analysis ID: 553E2019 SSA
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Product Use / Uso del Producto
Spanish

SISTEMA DE CIFOPLASTÍA PREVISTO PARA TRATAR LAS FRACTURAS VERTEBRALES

English

KYPHOPLASTY SYSTEM DESIGNED TO TREAT VERTEBRAL FRACTURES

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
SISTEMA DE CIFOPLASTÍA
Trade Name (English)
KYPHOPLASTY SYSTEM
Registration Information
Analysis ID
553E2019 SSA
Registration Date
March 15, 2019
Manufacturer / Fabricante
Name (English)
TRAUMASERVICE INTERNACIONAL, S.A. DE C.V.