NEURAMIS® LIGHT LIDOCAINE - COFEPRIS Registration 726C2022 SSA
Access comprehensive regulatory information for NEURAMIS® LIGHT LIDOCAINE (NEURAMIS® LIGHT LIDOCAINE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 726C2022 SSA and manufactured by EMERGO,S.DER.L.DE C.V.. The device was registered on August 03, 2022.
This page provides complete registration details including product type (II.PROSTHESES, 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.
NEURAMIS® LIGHT LIDOCAINE ESTÁ DISEÑADO PARAINYECTARSE EN LA DERMIS PARA EL TRATAMIENTO DEARRUGASFINAS,LARESTAURACIÓNDELHIDROBALANCEDELAPIELYLAMEJORADELAESTRUCTURAYLAELASTICIDADDELAPIEL.LAPRESENCIADELIDOCAÍNAESTÁDESTINADAA RED
NEURAMIS LIGHT LIDOCAINE IS DESIGNED TO BE INJECTED INTO THE DERMIS® FOR THE TREATMENT OF FINE WRINKLES, RESTORATION OF THE HYDROBALANCE OF THE SKIN AND IMPROVEMENT OF THE STRUCTURE AND ELASTICITY OF THE SKIN. THE presence of idocaine is intended for RED