PRECISION
LOS DISPOSITIVOS DE LA FAMILIA PRECISIONESTÁN INDICADOS COMO AYUDA PARA ELCONTROLDELDOLORCRÓNICORESISTENTEALTRATAMIENTO.
DEVICES IN THE PRECISION FAMILY ARE INDICATED AS AN AID TO THE MANAGEMENT OF TREATMENT-RESISTANT CHRONIC PAIN.
- 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)
- ESTIMULADOR IMPLANTABLE DEMÉDULA ESPINAL
- Trade Name (English)
- IMPLANTABLE SPINAL CORD STIMULATOR
- Analysis ID
- 1483C2020 SSA
- Registration Date
- October 29, 2020
- Name (Spanish)
- BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.
- Name (English)
- BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for PRECISION (PRECISION) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1483C2020 SSA and manufactured by BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.. The device was registered on October 29, 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.