Saudi Arabia SFDA registration ME0000000908SFDAA02492
TARGON
Saudi Arabia·Medical Device·Aesculap AG·Class IActiveProduct information
surgical orthopaedic prosthesis
Product use
The instrument set was designed specifically for implanting Aesculap Targon® implants.
It provides all instruments necessary for preparing the bone and the implant seat for insertion of an Aesculap
Targon® implant for a given indication.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000908SFDAA02492
- Authorization ID
- MDMA-1-2019-3182
- Status
- Active
- Expire Date
- July 09, 2025
Manufacturer
- Manufacturer Name
- Aesculap AG
Model information
- Model ID(s)
- KH399T KH534P
Product accessories
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About this record
Access comprehensive regulatory information for TARGON 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 ME0000000908SFDAA02492 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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