NEURAMIS® VOLUME LIDOCAINE
Mexico·Clase III·II.PROSTHESES, ORTHOSES AND FUNCTIONAL AIDS·EMERGO,S.DER.L.DE C.V.·Registered August 04, 2022NEURAMIS® 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
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II.PROTESIS,ÓRTESISYAYUDASFUNCIONALES
- Product Type (English)
- II.PROSTHESES, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- RELLENO DÉRMICO INYECTABLE
- Trade Name (English)
- INJECTABLE DERMAL FILLER
- Analysis ID
- 0731C2022 SSA
- Registration Date
- August 04, 2022
- Name (Spanish)
- EMERGO,S.DER.L.DE C.V.
- Name (English)
- EMERGO,S.DER. L.DE C.V.
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.