f2b1d5425849fefac08defa99d09e2d3
Hi-Flex Femoral Trials Asymmetric
EXACTECH INC.·I·Ecuador ARCSA·Registered December 14, 2015
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
Manufacturer
- Name
- EXACTECH INC.
- 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
Product use
IMPLANTATION OF KNEE PROSTHESIS OPTETRAK EXACTECH
About this record
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.