MK trial femoral spacer posterior - ARCSA Registration 9f5d108ca570eb97bd8d7f0b73a281fd
Access comprehensive regulatory information for MK trial femoral spacer posterior in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 9f5d108ca570eb97bd8d7f0b73a281fd and manufactured by IMPLANTCAST GMBH. The device was registered on December 08, 2022.
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
9f5d108ca570eb97bd8d7f0b73a281fd
MK trial femoral spacer posterior
ARCSA ID: 9f5d108ca570eb97bd8d7f0b73a281fd
Device Classification
Risk Class
I
Product Type
Invasive
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF PROSTHESIS, ORTHOPEDIC
Registration Information
Analysis ID
9f5d108ca570eb97bd8d7f0b73a281fd
Registration Date
December 08, 2022
Expiration Date
December 08, 2027
Product Use
FRACTURE FIXATION
Manufacturer
Product Owner
Name
IMPLANTCAST GMBH
Country
GERMANY
Authorized Representative