5F ADROIT® Guiding Catheter
- Risk class
- IV
- Product type
- Invasive
- Brand name
- ADROIT®
- Commercial name
- Vascular catheters for guidance.
- Sterilization method
- ETHYLENE OXIDE (EO)
- Analysis ID
- 49f4f40eebe12329449848e0166cca4d
- Registration date
- April 20, 2018
- Expiration date
- April 20, 2023
- Creation date
- October 22, 2020
- City
- CIUDAD JUAREZ
- Country
- MEXICO
- Address
- SANTIAGO TRONCOSO 808, PARQUE INDUSTRIAL SALVACAR, CIUDAD JUAREZ, CHIHUAHUA CP 32574, MEXICO
- Name
- CORDIS CORPORATION
- Country
- UNITED STATES
- Address
- AV ORELLANA ESQ E9-195 AND AV DECEMBER 6
- Phone
- 22563540
IT ALLOWS THE INTRAVASCULAR INTRODUCTION OF INTERVENTION/DIAGNOSTIC DEVICES IN THE CORONARY OR PERIPHERAL VASCULAR SYSTEMS.
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.