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RESCUENET. - COFEPRIS Registration 314C2021 SSA

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.

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COFEPRIS Official Data
Clase II
314C2021 SSA
RESCUENET.
COFEPRIS Analysis ID: 314C2021 SSA
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Product Use / Uso del Producto
Spanish

ESTE DISPOSITIVO ESTÁ DISEÑADO PARAUTILIZARSE EN LA EXTRACCIÓNENDOSCÓPICA DE CUERPOS EXTRAÑOS,BOLOS ALIMENTICIOS, FRAGMENTOS DETEJIDO Y TEJIDO EXTIRPADO COMO PÓLIPOS.

English

THIS DEVICE IS DESIGNED FOR USE IN THE ENDOSCOPIC REMOVAL OF FOREIGN BODIES, FOOD BOLUSES, TISSUE FRAGMENTS AND TISSUE REMOVED AS POLYPS.

Device Classification
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.
Registration Information
Analysis ID
314C2021 SSA
Registration Date
February 24, 2021
Manufacturer / Fabricante
Name (English)
BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.