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TARGON - SFDA Registration ME0000000908SFDAA02492

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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SFDA Official Data
Class I
ME0000000908SFDAA02492
TARGON
SFDA Registration: ME0000000908SFDAA02492
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Product Information

surgical orthopaedic prosthesis

Product Use

The instrument set was designed specifically for implanting Aesculap Targonยฎ implants. It provides all instruments necessary for preparing the bone and the implant seat for insertion of an Aesculap Targonยฎ 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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