RESCUENET.
ESTE DISPOSITIVO ESTÁ DISEÑADO PARAUTILIZARSE EN LA EXTRACCIÓNENDOSCÓPICA DE CUERPOS EXTRAÑOS,BOLOS ALIMENTICIOS, FRAGMENTOS DETEJIDO Y TEJIDO EXTIRPADO COMO PÓLIPOS.
THIS DEVICE IS DESIGNED FOR USE IN THE ENDOSCOPIC REMOVAL OF FOREIGN BODIES, FOOD BOLUSES, TISSUE FRAGMENTS AND TISSUE REMOVED AS POLYPS.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- DISPOSITIVO DE EXTRACCIÓN PORENDOSCOPÍA.
- Trade Name (English)
- PORENDOSCOPY EXTRACTION DEVICE.
- Analysis ID
- 314C2021 SSA
- Registration Date
- February 24, 2021
- Name (Spanish)
- BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.
- Name (English)
- BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for RESCUENET. (RESCUENET.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 314C2021 SSA and manufactured by BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.. The device was registered on February 24, 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.