AQWIRE HYDROPHILIC GUIDEWIRE - COFEPRIS Registration 934C2018 SSA
Access comprehensive regulatory information for AQWIRE HYDROPHILIC GUIDEWIRE (AQWIRE HYDROPHILIC GUIDEWIRE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 934C2018 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on April 12, 2018.
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.
DISPOSITIVO DISEÑADO PARA FACILITAR LA COLOCACIÓN DE DISPOSITIVOS DURANTE LOS PROCEDIMIENTOS DE INTERVENCIÓN Y DE DIAGNÓSTICO EN LA VASCULATURA PERIFÉRICA
DEVICE DESIGNED TO FACILITATE THE PLACEMENT OF DEVICES DURING INTERVENTIONAL AND DIAGNOSTIC PROCEDURES IN THE PERIPHERAL VASCULATURE