AIR - COFEPRIS Registration 1296C2018 SSA
Access comprehensive regulatory information for AIR (AIR) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1296C2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on June 01, 2018.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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 SISTEMA DE REPARACIÓN DE MENISCO COMPLETAMENTE INTERNO AIR ESTÁ PREVISTO PARA SU USO COMO DISPOSITIVO DE RETENCIÓN DE SUTURAS CON EL FIN DE FACILITAR LOS PROCEDIMIENTOS PERCUTÁNEOS O ENDOSCÓPICOS EN TEJIDO BLANDO. EL SISTEMA DE REPARACIÓN DE MENISCO AI
THE AIR ALL-INTERNAL MENISCUS REPAIR SYSTEM IS INTENDED FOR USE AS A SUTURE RETENTION DEVICE TO FACILITATE PERCUTANEOUS OR ENDOSCOPIC SOFT TISSUE PROCEDURES. THE AI MENISCUS REPAIR SYSTEM