Hi-Flex Tibial Insert Trials. - ARCSA Registration 5aeaa2361cd0e1950fc4f3215ad02276
Access comprehensive regulatory information for Hi-Flex Tibial Insert Trials. in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 5aeaa2361cd0e1950fc4f3215ad02276 and manufactured by EXACTECH INC.. The device was registered on December 14, 2015.
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
5aeaa2361cd0e1950fc4f3215ad02276
Hi-Flex Tibial Insert Trials.
ARCSA ID: 5aeaa2361cd0e1950fc4f3215ad02276
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
Optetrak
Commercial Name
Instruments for implantation of Prosthetics, Orthopedic
Registration Information
Analysis ID
5aeaa2361cd0e1950fc4f3215ad02276
Registration Date
December 14, 2015
Expiration Date
December 14, 2025
Product Use
IMPLANTATION OF KNEE PROSTHESIS OPTETRAK EXACTECH
Manufacturer
Product Owner
Name
EXACTECH INC.
Country
UNITED STATES
Authorized Representative
Address
AV. 12 DE OCTUBRE N24-739 Y AV COLON TORRE BOREAL PISO 1 OF 103
Phone
23945303