MaXcess® MAS TLIF Blade - ARCSA Registration 6a9422555bd1f16ce76a706f1ea98848
Access comprehensive regulatory information for MaXcess® MAS TLIF Blade in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 6a9422555bd1f16ce76a706f1ea98848 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
6a9422555bd1f16ce76a706f1ea98848
MaXcess® MAS TLIF Blade
ARCSA ID: 6a9422555bd1f16ce76a706f1ea98848
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
NUVASIVE®
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF ORTHOPEDIC PROSTHESES
Registration Information
Analysis ID
6a9422555bd1f16ce76a706f1ea98848
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