HEMODIALIZADORES DIAPES - COFEPRIS Registration 960C2019 SSA
Access comprehensive regulatory information for HEMODIALIZADORES DIAPES (HEMODIALIZADORES DIAPES) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 960C2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on May 09, 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 TRATAMIENTO 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 TREATMENT IN CONDITIONS OF ACUTE AND CHRONIC RENAL FAILURE. BLOOD PURIFICATION TREATMENTS IN CASE OF ACUTE POISONING WITH DIALYZABLE SUBSTANCES