ANYPLUS PEEK CAGE SYSTEMINSTRUMENTS - COFEPRIS Registration 237E2022 SSA
Access comprehensive regulatory information for ANYPLUS PEEK CAGE SYSTEMINSTRUMENTS (ANYPLUS PEEK CAGE SYSTEMINSTRUMENTS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 237E2022 SSA and manufactured by EMERGO,S.DER.L.DE C.V.. The device was registered on March 17, 2022.
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.
CONJUNTODEINSTRUMENTOSQUIRÚRGICOSDISEÑADOSPARALACOLOCACIÓNDEDISPOSITIVOSANYPLUSLUMBARPEEK CAGE(PLIF,T-PLIF,TLIF,ALIF)YANYPLUSCERVICALPEEKCAGEDEGSMEDICAL,QUESEUTILIZANDEACUERDOCON LA TÉCNICA QUIRÚRGICA CORRESPONDIENTE
SET OF SURGICAL INSTRUMENTS DESIGNED FOR THE PLACEMENT OF DEVICES AND PLUSLUMBARPEEK CAGE (PLIF, T-PLIF, TLIF, ALIF) YANY PLUSCERVICALPEEK CAGEDEGSMEDICAL, WHICH ARE USED ACCORDING TO THE CORRESPONDING SURGICAL TECHNIQUE