XLIF® Shaft - ARCSA Registration 8f5c9083d5ffbc9cd5317bfd731a6cee
Access comprehensive regulatory information for XLIF® Shaft in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 8f5c9083d5ffbc9cd5317bfd731a6cee 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
8f5c9083d5ffbc9cd5317bfd731a6cee
XLIF® Shaft
ARCSA ID: 8f5c9083d5ffbc9cd5317bfd731a6cee
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
NUVASIVE®
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF ORTHOPEDIC PROSTHESES
Registration Information
Analysis ID
8f5c9083d5ffbc9cd5317bfd731a6cee
Registration Date
November 12, 2016
Expiration Date
November 12, 2026
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