Pure Global

5F ADROIT® Guiding Catheter - ARCSA Registration 49f4f40eebe12329449848e0166cca4d

Access comprehensive regulatory information for 5F ADROIT® Guiding Catheter in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 49f4f40eebe12329449848e0166cca4d and manufactured by CARDINAL HEALTH MEXICO 244 S DE RL DE CV. The device was registered on April 20, 2018.

This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

Free Database
Powered by Pure Global AI
ARCSA Official Data
IV
49f4f40eebe12329449848e0166cca4d
5F ADROIT® Guiding Catheter
ARCSA ID: 49f4f40eebe12329449848e0166cca4d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
ADROIT®
Commercial Name
Vascular catheters for guidance.
Sterilization Method
ETHYLENE OXIDE (EO)
Registration Information
Analysis ID
49f4f40eebe12329449848e0166cca4d
Registration Date
April 20, 2018
Expiration Date
April 20, 2023
Creation Date
October 22, 2020
Product Use

IT ALLOWS THE INTRAVASCULAR INTRODUCTION OF INTERVENTION/DIAGNOSTIC DEVICES IN THE CORONARY OR PERIPHERAL VASCULAR SYSTEMS.

Manufacturer
City
CIUDAD JUAREZ
Country
MEXICO
Address
SANTIAGO TRONCOSO 808, PARQUE INDUSTRIAL SALVACAR, CIUDAD JUAREZ, CHIHUAHUA CP 32574, MEXICO
Product Owner
Name
CORDIS CORPORATION
Country
UNITED STATES
Authorized Representative
Address
AV ORELLANA ESQ E9-195 AND AV DECEMBER 6
Phone
22563540