Mexico COFEPRIS registration 63C2020 SSA

VERCISE GEVIA

EN: VERCISE GEVIA
Mexico flagMexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.·Registered February 04, 2020
Product Use / Uso del Producto
Spanish

VERCISE GEVIAESTÁ INDICADOPARA SUUSOEN: -ESTIMULACIÓNUNILATERALOBILATERALDEL NÚCLEO SUBTALÁMICO (STN) O GLOBOPÁLIDOINTERNO(GPI)PARAENFERMEDADDEPARKINSON RESPONSIVA A LEVODOPA NOCONTROLADA ADECUADAMENTE CONMEDICACIÓN. - ESTIMULACIÓN UNILATERAL OBILATERALDELNÚCLEOSUBTALÁMICO(STN)OGLOBOPÁLIDOINTERNO(GPI)PARADISTONIAPRIMARIA Y SECUNDARIA INTRATABLE, PARAPERSONAS A PARTIR DE 7 AÑOS. -ESTIMULACIÓNTALÁMICAPARALASUPRESIÓNDE TEMBLOR CONTROLADOINADECUADAMENTE.

English

VERCISE GEVIA IS INDICATED FOR SUUSOIN: -UNILATERAL BILATERAL STIMULATION OF THE SUBTHALAMIC NUCLEUS (STN) OR GLOBOPALLIDUS INTERNAL (PG) FOR LEVODOPA-RESPONSIVE PARKINSON'S DISEASE NOT ADEQUATELY CONTROLLED WITH MEDICATION. - UNILATERAL OR BILATERAL STIMULATION OF THE SUBTHALAMIC NUCLEUS (STN) OR INTERNAL GLOBOPALLID (GPI) FOR INTRACTABLE PRIMARY AND SECONDARY PARADYSTONIA, FOR PEOPLE FROM 7 YEARS OLD. -THALAMIC STIMULATION FOR THE SUPPRESSION OF INADEQUATELY CONTROLLED TREMOR.

Device classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
NEUROESTIMULADOR
Trade Name (English)
NEUROESTIMULADOR
Registration information
Analysis ID
63C2020 SSA
Registration Date
February 04, 2020
Manufacturer / Fabricante
Name (English)
BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.
About this record

Access comprehensive regulatory information for VERCISE GEVIA (VERCISE GEVIA) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 63C2020 SSA and manufactured by BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.. The device was registered on February 04, 2020.

This page provides complete registration details including product type (II. PROSTHETICS, 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.

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