Saudi Arabia SFDA registration ME0000000908SFDAA01895
PROCART HANDLE
Saudi Arabia·Medical Device·Aesculap AG·Class IActiveProduct information
surgical orthopaedic prosthesis
Product use
The OCT instrument set (OsteoChondral Transplantation) is used for the treatment of cartilage defects at the femoral
condyles. The OCT instrument set is used to make osteochondral plugs and recipient drill holes.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000908SFDAA01895
- Authorization ID
- MDMA-1-2019-3182
- Status
- Active
- Expire Date
- July 09, 2025
Manufacturer
- Manufacturer Name
- Aesculap AG
Model information
- Model ID(s)
- FR600R
Product accessories
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About this record
Access comprehensive regulatory information for PROCART HANDLE in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000908SFDAA01895 and manufactured by Aesculap AG.
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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