PAJUNK® RADIOFREQUENCYTHERMAL LESIONING CANNULA. - COFEPRIS Registration 1197C2021 SSA
Access comprehensive regulatory information for PAJUNK® RADIOFREQUENCYTHERMAL LESIONING CANNULA. (PAJUNK® RADIOFREQUENCYTHERMAL LESIONING CANNULA.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1197C2021 SSA and manufactured by EMERGO,S.DER.L.DEC.V.. The device was registered on October 08, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
LAS CÁNULAS PAJUNK® RADIOFREQUENCYTHERMAL LESIONING CANNULA SONUTILIZADAS PARA LA INTERRUPCIÓNTRANSITORIA DE LA CONDUCTIVIDAD DENERVIOS, PARA PACIENTES CON DOLORCRÓNICO QUE NO LOGRARON MEJORÍAMEDIANTE TENS, FISIOTERAPIA Y/O TERAPIAMANUAL.
PAJUNK® RADIOFREQUENCYTHERMAL LESIONING CANNULA CANNULAS ARE USED FOR TRANSIENT INTERRUPTION OF NERVE CONDUCTIVITY FOR PATIENTS WITH CHRONIC PAIN WHO DID NOT ACHIEVE IMPROVEMENT BY TENS, PHYSIOTHERAPY AND/OR MANUAL THERAPY.