STRYKER INSTRUMENTAL - COFEPRIS Registration 357E2019 SSA
Access comprehensive regulatory information for STRYKER INSTRUMENTAL (STRYKER INSTRUMENTAL) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 357E2019 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on February 22, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 CONJUNTO DE EMPUJADOR DE NUDOS / CORTADOR DE SUTURA Y CÁNULA RANURADA STRYKER 2-0 ESTÁ DESTINADO A USARSE EN APLICACIONES ARTROSCÓPICAS DE MENISCO.
THE STRYKER 2-0 SLOTTED CANNUTE AND SUTURE CUTTER PUSHER/CUTTER ASSEMBLY IS INTENDED FOR USE IN ARTHROSCOPIC MENISCUS APPLICATIONS.