NEURAMIS® DEEP LIDOCAINE - COFEPRIS Registration 0717C2022 SSA
Access comprehensive regulatory information for NEURAMIS® DEEP LIDOCAINE (NEURAMIS® DEEP 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 0717C2022 SSA and manufactured by EMERGO,S.DER.L.DE C.V.. The device was registered on August 02, 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®DEEPLIDOCAINEESTÁDISEÑADOPARASERINYECTADO EN LA DERMIS PARA EL TRATAMIENTO DEARRUGAS Y PLIEGUES EN LA PARTE BAJA DE LA CARA,ESPECIALMENTE DE LOS PLIEGUES NASOGENIANOS. LAPRESENCIA DE LIDOCAÍNA TIENE LA INTENCIÓN DEREDUCIR EL DOLOR DEL
NEURAMIS DEEPLIDOCAINE IS DESIGNED TO BE INJECTED INTO THE DERMIS®FOR THE TREATMENT OF WRINKLES AND FOLDS IN THE LOWER FACE, ESPECIALLY THE NASOLABIAL FOLDS. THE PRESENCE OF LIDOCAINE IS INTENDED TO REDUCE THE PAIN OF THE