HEMODIALIZADORES PHYLTHER® - COFEPRIS Registration 896C2019 SSA
Access comprehensive regulatory information for HEMODIALIZADORES PHYLTHER® (HEMODIALIZADORES PHYLTHER®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 896C2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on May 02, 2019.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
DISPOSITIVOS DISEÑADOS PARA TRATAMIENTOS DE HEMODIÁLISIS EN CONDICIONES DE FALLA RENAL AGUDA Y CRÓNICA. TRATAMIENTOS DE DEPURACIÓN DE SANGRE EN CASO DE INTOXICACIÓN AGUDA CON SUSTANCIAS DIALIZABLES.
DEVICES DESIGNED FOR HEMODIALYSIS TREATMENTS IN CONDITIONS OF ACUTE AND CHRONIC RENAL FAILURE. BLOOD PURIFICATION TREATMENTS IN CASE OF ACUTE POISONING WITH DIALYZABLE SUBSTANCES.