K-Wire, Blunt, 1.5 X 350 MM - ARCSA Registration ce7820a93fd744877f658df030e7d0c8
Access comprehensive regulatory information for K-Wire, Blunt, 1.5 X 350 MM in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID ce7820a93fd744877f658df030e7d0c8 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.
Free Database
Powered by Pure Global AI
ARCSA Official Data
I
ce7820a93fd744877f658df030e7d0c8
K-Wire, Blunt, 1.5 X 350 MM
ARCSA ID: ce7820a93fd744877f658df030e7d0c8
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
tedan
Commercial Name
13-373 Retractors
Registration Information
Analysis ID
ce7820a93fd744877f658df030e7d0c8
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