INTERJECT - COFEPRIS Registration 666C2021 SSA
Access comprehensive regulatory information for INTERJECT (INTERJECT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 666C2021 SSA and manufactured by BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.. The device was registered on April 16, 2021.
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 CATÉTER CON AGUJA INTERJECT PARATRATAMIENTOINYECTABLESEUTILIZAPARALAINYECCIÓNENDOSCÓPICAENLAMUCOSAY LA SUBMUCOSA DIGESTIVAS
THE INTERJECT NEEDLE CATHETER FOR INJECTABLE TREATMENT IS USED FOR ENDOSCOPIC INJECTION INTO THE DIGESTIVE MUCOSA AND SUBMUCOSA