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Helix-T Screw, Fixed Self-Drill - ARCSA Registration f4931c5bd38c3f67918b6a0f40b5bdc9

Access comprehensive regulatory information for Helix-T Screw, Fixed Self-Drill in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID f4931c5bd38c3f67918b6a0f40b5bdc9 and manufactured by NUVASIVE INC.. The device was registered on March 31, 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
IV
f4931c5bd38c3f67918b6a0f40b5bdc9
Helix-T Screw, Fixed Self-Drill
ARCSA ID: f4931c5bd38c3f67918b6a0f40b5bdc9
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
NUVASIVE
Commercial Name
ORTHOPEDIC INTERNAL FIXATION SYSTEMS FOR SPINE
Registration Information
Analysis ID
f4931c5bd38c3f67918b6a0f40b5bdc9
Registration Date
March 31, 2016
Expiration Date
March 31, 2026
Product Use

THE NUVASIVE HELIX ACP SYSTEM IS DESIGNED FOR FIXING SCREWS IN THE ANTERIOR AREA OF THE CERVICAL SPINE. THESE IMPLANTS ARE DESIGNED TO PROVIDE STABILITY AS AN ADJUNCT TO CERVICAL FUSION.

Manufacturer
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