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OVAION IX - COFEPRIS Registration 2092C2018 SSA

Access comprehensive regulatory information for OVAION IX (OVAION IX) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2092C2018 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on August 28, 2018.

This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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 III
2092C2018 SSA
OVAION IX
COFEPRIS Analysis ID: 2092C2018 SSA
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Product Use / Uso del Producto
Spanish

PARA EL TRATAMIENTO DE ANEURISMAS Aร“RTICOS ABDOMINALES PARA LA REPARACIร“N ENDOVASCULAR

English

FOR THE TREATMENT OF ABDOMINAL AORTIC ANEURYSMS FOR ENDOVASCULAR REPAIR

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ร“RTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
STENT ABDOMINAL
Trade Name (English)
STENT ABDOMINAL
Registration Information
Analysis ID
2092C2018 SSA
Registration Date
August 28, 2018
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL S.A. DE C.V.