Screw Ø1.8 Cortical - ARCSA Registration 226fbfef7413ea854964e6d2b5364401
Access comprehensive regulatory information for Screw Ø1.8 Cortical in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 226fbfef7413ea854964e6d2b5364401 and manufactured by JEIL MEDICAL CORPORATION. The device was registered on August 18, 2021.
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
III
226fbfef7413ea854964e6d2b5364401
Screw Ø1.8 Cortical
ARCSA ID: 226fbfef7413ea854964e6d2b5364401
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
JEIL
Commercial Name
Orthopedic External Fixation Systems for Fractures
Registration Information
Analysis ID
226fbfef7413ea854964e6d2b5364401
Registration Date
August 18, 2021
Expiration Date
August 18, 2026
Product Use
INTENDED FOR USE FOR TEMPORARY FIXATION, CORRECTION OR STABILIZATION OF BONES
Manufacturer
City
SEOUL
Country
KOREA, REPUBLIC OF
Address
702, 703, 704, 705, 706, 804, 805, 807, 812, 815-HO, 55, DIGITAL-RO 34-GIL, GUROGU, SEOUL, REP. OF KOREA & 380, BEOMAN-RO, SIHEUNG-SI, GYEONGGI-DO, 14928, REP. OF KOREA.
Product Owner
Name
JEIL MEDICAL CORPORATION
Country
KOREA, REPUBLIC OF
Authorized Representative