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MK FB trial PE-insert - ARCSA Registration 8564c39cac387fb9d1db15f26069fe18

Access comprehensive regulatory information for MK FB trial PE-insert in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 8564c39cac387fb9d1db15f26069fe18 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
8564c39cac387fb9d1db15f26069fe18
MK FB trial PE-insert
ARCSA ID: 8564c39cac387fb9d1db15f26069fe18
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Device Classification
Risk Class
I
Product Type
Invasive
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF PROSTHESIS, ORTHOPEDIC
Registration Information
Analysis ID
8564c39cac387fb9d1db15f26069fe18
Registration Date
December 08, 2022
Expiration Date
December 08, 2027
Product Use

FRACTURE FIXATION

Manufacturer
Country
GERMANY
Address
LUENEBURGER SCHANZE 26 - 21614
Product Owner
Name
IMPLANTCAST GMBH
Country
GERMANY
Authorized Representative
Address
OF. COLON 1133 Y OF. AMAZON
Phone
22554297