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MaXcess Annulotomy Knife - ARCSA Registration f738f3c8b03839faf5936691035b10f0

Access comprehensive regulatory information for MaXcess Annulotomy Knife in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID f738f3c8b03839faf5936691035b10f0 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
f738f3c8b03839faf5936691035b10f0
MaXcess Annulotomy Knife
ARCSA ID: f738f3c8b03839faf5936691035b10f0
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Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
NUVASIVE®
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF ORTHOPEDIC PROSTHESES
Registration Information
Analysis ID
f738f3c8b03839faf5936691035b10f0
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
City
SAN DIEGO CALIFORNIA
Country
UNITED STATES
Address
7475 LUSK BLVD
Product Owner
Name
NUVASIVE INC.
Country
UNITED STATES
Authorized Representative
Address
ROCA 152 AND AV 12 DE OCTUBRE
Phone
22522087