K-Wire, Sharp, 1.4 X 230 MM - ARCSA Registration 93e2fa02700262aa91f85b2d9d23fde0
Access comprehensive regulatory information for K-Wire, Sharp, 1.4 X 230 MM in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 93e2fa02700262aa91f85b2d9d23fde0 and manufactured by TEDAN SURGICAL INNOVATIONS, LLC. The device was registered on July 02, 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
I
93e2fa02700262aa91f85b2d9d23fde0
K-Wire, Sharp, 1.4 X 230 MM
ARCSA ID: 93e2fa02700262aa91f85b2d9d23fde0
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
tedan
Commercial Name
13-373 Retractors
Registration Information
Analysis ID
93e2fa02700262aa91f85b2d9d23fde0
Registration Date
July 02, 2021
Expiration Date
July 02, 2026
Product Use
SURGICAL APPROACH SYSTEM
Manufacturer
Country
UNITED STATES
Address
12615 W. AIRPORT BLVD, SUITE 200 SUGAR LAND, TX 77478 UNITED STATES
Product Owner
Name
TEDAN SURGICAL INNOVATIONS, LLC
Country
UNITED STATES
Authorized Representative
Address
PICHINCHA / QUITO / QUITO METROPOLITAN DISTRICT / REPUBLIC OF EL SALVADOR E9-24 AND AV DE LOS SHYRIS
Phone
23332297