NEURAMIS® VOLUME LIDOCAINE - COFEPRIS Registration 0731C2022 SSA
Access comprehensive regulatory information for NEURAMIS® VOLUME LIDOCAINE (NEURAMIS® VOLUME 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 0731C2022 SSA and manufactured by EMERGO,S.DER.L.DE C.V.. The device was registered on August 04, 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® VOLUME LIDOCAINE ESTÁ DISEÑADO PARAINYECTARSE EN LA DERMIS PROFUNDA, PERIOSTEASUPERIOR O SUBCUTÁNEA PARA EL TRATAMIENTO DEARRUGASYPLIEGUESENLACARA,MEJILLAS,AUMENTODEMENTÓNYDARFORMAALOSCONTORNOSDELACARA.LAPRESENCIA DE LIDOC
NEURAMIS VOLUME LIDOCAINE IS DESIGNED TO BE INJECTED INTO THE DEEP, UPPER PERIOSEAL OR SUBCUTANEOUS DERMIS® FOR THE TREATMENT OF WRINKLES AND FOLDS IN THE FACE, CHEEKS, CHIN AUGMENTATION AND SHAPING THE CONTOURS OF THE FACE. THE PRESENCE OF LIDOC