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ECLIPSE 2L / COPERNIC 2L - COFEPRIS Registration 884C2019 SSA

Access comprehensive regulatory information for ECLIPSE 2L / COPERNIC 2L (ECLIPSE 2L / COPERNIC 2L) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 884C2019 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on April 30, 2019.

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 III
884C2019 SSA
ECLIPSE 2L / COPERNIC 2L
COFEPRIS Analysis ID: 884C2019 SSA
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Product Use / Uso del Producto
Spanish

DISPOSITIVO DISEร‘ADO PARA LA OCLUSIร“N TEMPORAL DE LA VASCULATURA PERIFร‰RICA Y LA NEUROVASCULATURA

English

DEVICE DESIGNED FOR TEMPORARY OCCLUSION OF PERIPHERAL VASCULATURE AND NEUROVASCULATURE

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. MATERIALES QUIRรšRGICOS Y DE CURACIร“N
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
CATร‰TER BALร“N DE DOBLE LUMEN
Trade Name (English)
DOUBLE LUMEN BALLOON CATHETER
Registration Information
Analysis ID
884C2019 SSA
Registration Date
April 30, 2019
Manufacturer / Fabricante
Name (English)
ISA HEALTH, S.A DE C.V.