ULTRAEZ®. - COFEPRIS Registration 525R2021 SSA
Access comprehensive regulatory information for ULTRAEZ®. (ULTRAEZ®.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 525R2021 SSA and manufactured by EMERGO,S.DER.L.DEC.V.. The device was registered on March 26, 2021.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.
EL GEL DESENSIBILIZANTE ULTRAEZ®PROPORCIONA UN BARNIZ EN FORMA DEPELÍCULA PARA DIENTES SENSIBLES,SELLANDOLOSTÚBULOSDENTINARIOSDELADENTINA EXPUESTA Y DE OTRAS ZONASDONDELASENSIBILIDADPOST-OPERATORIAESPROBLEMÁTICA.ELPRODUCTOPUEDESERUTILIZADO PROFESIONALMENTE EN ELCONSULTORIODENTALOSERENTREGADOALPACIENTEPARATRATAMIENTODOMICILIARIODE LA SENSIBILIDAD DENTAL.
THE ULTRAEZ®DESENSITIZING GEL PROVIDES A VARNISH IN THE FORM OF A FILM FOR SENSITIVE TEETH, SEALING THE DENTINAL TUBULES OF EXPOSED LADENTINE AND OTHER AREASWHERE POSTOPERATIVE SENSITIVITY IS PROBLEMATIC. THE PRODUCT CAN BE USED PROFESSIONALLY IN THE DENTAL OFFICE AND DELIVERED TO THE PATIENT FOR HOME TREATMENT OF TOOTH SENSITIVITY.