MEDIGUARD ES®. - COFEPRIS Registration 908C2019 SSA
Access comprehensive regulatory information for MEDIGUARD ES®. (MEDIGUARD ES®.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 908C2019 SSA and manufactured by MEDLINE MÉXICO, S. DE R.L. 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.
INDICADOS PARA LA EXPLORACIÓN DE PACIENTES EN CONSULTORIOS, CLÍNICAS Y HOSPITALES; MUESTREO, CURACIONES, PROCEDIMIENTOS ODONTOLÓGICOS; PARA MANIPULAR DISPOSITIVOS MÉDICOS Y PRODUCTOS Y EVITAR CONTACTO CON LA PIEL.
INDICATED FOR THE EXAMINATION OF PATIENTS IN OFFICES, CLINICS AND HOSPITALS; SAMPLING, CURES, DENTAL PROCEDURES; TO HANDLE MEDICAL DEVICES AND PRODUCTS AND AVOID SKIN CONTACT.