INSUFLADOR FM134 (50L) - COFEPRIS Registration 1972E2019 SSA
Access comprehensive regulatory information for INSUFLADOR FM134 (50L) (INSUFLADOR FM134 (50L)) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1972E2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on October 10, 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.
EL APARATO INSUFLADOR 50L SE UTILIZA PARA CREAR UNA CAVIDAD MEDIANTE LA INSUFLACIÓN DE CO2 DURANTE EL DIAGNÓSTICO Y/O LA LAPAROSCOPÍA TERAPÉUTICA.
THE 50L INSUFFLATOR DEVICE IS USED TO CREATE A CAVITY BY INSUFFLATION CO2 DURING DIAGNOSIS AND/OR THERAPEUTIC LAPAROSCOPY.