HelixAR System - ARCSA Registration e9e5e9ff939bc3335d8b75a04acbffcf
Access comprehensive regulatory information for HelixAR System in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID e9e5e9ff939bc3335d8b75a04acbffcf and manufactured by CONMED CORPORATION. The device was registered on January 16, 2023.
This page provides complete registration details including product type (Active), 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
III
e9e5e9ff939bc3335d8b75a04acbffcf
HelixAR System
ARCSA ID: e9e5e9ff939bc3335d8b75a04acbffcf
Device Classification
Risk Class
III
Product Type
Active
Brand Name
ConMed
Commercial Name
Units for Electrosurgery
Registration Information
Analysis ID
e9e5e9ff939bc3335d8b75a04acbffcf
Registration Date
January 16, 2023
Expiration Date
January 16, 2028
Product Use
ELECTROSURGICAL EQUIPMENT, WHICH USES A HIGH-FREQUENCY ELECTRIC CURRENT TO CUT TISSUE AND CONTROL BLEEDING THROUGH CLOTTING
Manufacturer
Product Owner
Name
CONMED CORPORATION
Country
UNITED STATES
Authorized Representative