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Armada Ti Connector, Cross Fixed - ARCSA Registration 1bf3ae699806d7d514bb178d60002234

Access comprehensive regulatory information for Armada Ti Connector, Cross Fixed in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 1bf3ae699806d7d514bb178d60002234 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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III
1bf3ae699806d7d514bb178d60002234
Armada Ti Connector, Cross Fixed
ARCSA ID: 1bf3ae699806d7d514bb178d60002234
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Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
ARMADA®
Commercial Name
Orthopedic Internal Fixation Systems for Spine
Registration Information
Analysis ID
1bf3ae699806d7d514bb178d60002234
Registration Date
March 31, 2016
Expiration Date
March 31, 2026
Product Use

SYSTEM OF SCREWS, BARS, HOOKS AND CONNECTORS TO IMMOBILIZE AND SPLINT THE VERTEBRAL SEGMENTS IN PATIENTS WITH MATURE SKELETON FOR THE TREATMENT OF DEFORMITIES OF THE THORACIC, LUMBAR AND SACRAL SPINE.

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