ANGIOJET PE - COFEPRIS Registration 1686C2019 SSA
Access comprehensive regulatory information for ANGIOJET PE (ANGIOJET ON) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1686C2019 SSA and manufactured by BOSTON SCIENTIFIC DE MÉXICO, S.A. DE C.V.. The device was registered on August 22, 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.
ANGIOJET PE ESTÁ INDICADO PARA SU USO EXCLUSIVO CON LA CONSOLA ANGIOJET ULTRA PARA SEPARAR Y ELIMINAR TROMBOS DE: • PRINCIPALES ARTERIAS PULMONARES Y LOBARES ≥ 6 MM DE DIÁMETRO. • PARA SU USO CON LA TÉCNICA ANGIOJET POWER PULSE EN EL CONTROL Y L
ANGIOJET PE IS INDICATED FOR USE ONLY WITH THE ANGIOJET ULTRA CONSOLE TO SEPARATE AND REMOVE THROMBI FROM: • MAIN PULMONARY AND LOBAR ARTERIES ≥ 6 MM IN DIAMETER. • FOR USE WITH THE ANGIOJET POWER PULSE TECHNIQUE ON THE CONTROL AND L