Mexico COFEPRIS registration 237E2022 SSA

ANYPLUS PEEK CAGE SYSTEMINSTRUMENTS

EN: ANYPLUS PEEK CAGE SYSTEMINSTRUMENTS
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·EMERGO,S.DER.L.DE C.V.·Registered March 17, 2022
Product Use / Uso del Producto
Spanish

CONJUNTODEINSTRUMENTOSQUIRÚRGICOSDISEÑADOSPARALACOLOCACIÓNDEDISPOSITIVOSANYPLUSLUMBARPEEK CAGE(PLIF,T-PLIF,TLIF,ALIF)YANYPLUSCERVICALPEEKCAGEDEGSMEDICAL,QUESEUTILIZANDEACUERDOCON LA TÉCNICA QUIRÚRGICA CORRESPONDIENTE

English

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

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
INSTRUMENTAL QUIRÚRGICOPARA ARTRODESIS VERTEBRAL
Trade Name (English)
SURGICAL INSTRUMENTS FOR SPINAL FUSION
Registration information
Analysis ID
237E2022 SSA
Registration Date
March 17, 2022
Manufacturer / Fabricante
Name (English)
EMERGO,S.DER. L.DE C.V.
About this record

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.

Free DatabasePowered by Pure Global AICOFEPRIS Official DataClase I