CoRoent XLW Trial, 10° - ARCSA Registration 8132ebc15b5568b2331d8ee83649f8c0
Access comprehensive regulatory information for CoRoent XLW Trial, 10° in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 8132ebc15b5568b2331d8ee83649f8c0 and manufactured by NUVASIVE INC. The device was registered on November 12, 2016.
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.
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ARCSA Official Data
I
8132ebc15b5568b2331d8ee83649f8c0
CoRoent XLW Trial, 10°
ARCSA ID: 8132ebc15b5568b2331d8ee83649f8c0
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
NUVASIVE®
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF ORTHOPEDIC PROSTHESES
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
8132ebc15b5568b2331d8ee83649f8c0
Registration Date
November 12, 2016
Expiration Date
November 12, 2026
Creation Date
May 10, 2021
Product Use
NUVASIVE'S GENERAL INSTRUMENTS ARE DEVICES THAT ARE USED MANUALLY AND ARE INDICATED FOR USE IN SPINAL SURGICAL PROCEDURES.
Manufacturer
Product Owner
Name
NUVASIVE INC.
Country
UNITED STATES
Authorized Representative