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Hi-Flex Femoral Trials Asymmetric - ARCSA Registration f2b1d5425849fefac08defa99d09e2d3

Access comprehensive regulatory information for Hi-Flex Femoral Trials Asymmetric in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID f2b1d5425849fefac08defa99d09e2d3 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.

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ARCSA Official Data
I
f2b1d5425849fefac08defa99d09e2d3
Hi-Flex Femoral Trials Asymmetric
ARCSA ID: f2b1d5425849fefac08defa99d09e2d3
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Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
Optetrak
Commercial Name
Instruments for implantation of Prosthetics, Orthopedic
Registration Information
Analysis ID
f2b1d5425849fefac08defa99d09e2d3
Registration Date
December 14, 2015
Expiration Date
December 14, 2025
Product Use

IMPLANTATION OF KNEE PROSTHESIS OPTETRAK EXACTECH

Manufacturer
Country
UNITED STATES
Address
2320 N.W. 66TH CT. GAINESVILLE-FLORIDA, USA 32653
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