EQUIPOS FLEXYA®
Mexico·Clase II·I. MEDICAL EQUIPMENT·KENDALL DE MÉXICO, S.A. DE C.V.·Registered July 16, 2019SISTEMA PARA TRATAMIENTOS EXTRACORPÓREOS DE DIÁLISIS Y HEMODIAFILTRACIÓN.
SYSTEM FOR EXTRACORPOREAL TREATMENTS OF DIALYSIS AND HEMODIAFILTRATION.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- EQUIPO Y ACCESORIOS PARA HEMODIÁLISIS
- Trade Name (English)
- HEMODIALYSIS EQUIPMENT AND ACCESSORIES
- Analysis ID
- 1341E2019 SSA
- Registration Date
- July 16, 2019
- Name (Spanish)
- KENDALL DE MÉXICO, S.A. DE C.V.
- Name (English)
- KENDALL DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for EQUIPOS FLEXYA® (FLEXYA® EQUIPMENT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1341E2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on July 16, 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.