TREVO® PRO 18 - COFEPRIS Registration 1656C2018 SSA
Access comprehensive regulatory information for TREVO® PRO 18 (TREVO® PRO 18) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1656C2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on June 29, 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.
EL MICROCATÉTER ESTÁ INDICADO PARA USARSE EN LA COLOCACIÓN SELECTIVA DE FLUIDOS Y OTROS DISPOSITIVOS O AGENTES EN LA NEUROVASCULATURA Y LA VASCULATURA PERIFÉRICA Y CORONARIA DURANTE PROCEDIMIENTOS TERAPÉUTICOS O DE DIAGNÓSTICO.
THE MICROCATHETER IS INDICATED FOR USE IN THE SELECTIVE PLACEMENT OF FLUIDS AND OTHER DEVICES OR AGENTS IN THE NEUROVASCULATURE AND PERIPHERAL AND CORONARY VASCULATURE DURING THERAPEUTIC OR DIAGNOSTIC PROCEDURES.