Saudi Arabia SFDA registration ME0000000535SFDAA00217

Cannulated Twist Drill

Saudi Arabia flagSaudi Arabia·Medical Device·Medartis AG·Class IIaActive
Product information
Instrument for making or enlarging a hole in bone or tooth
Product use
The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. The APTUS cannulated compression screws are used for bone fractures, osteotomies and arthrodesis.Twist drills are available for various APTUS system size for Drilling of bone.
Device classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration information
Registration ID
ME0000000535SFDAA00217
Authorization ID
MDMA-1-2020-0972
Status
Active
Expire Date
February 03, 2025
Manufacturer
Manufacturer Name
Medartis AG
Model information
Model ID(s)
A-3736 A-3738 A-3836 A-3838
Product accessories
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About this record

Access comprehensive regulatory information for Cannulated Twist Drill in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000000535SFDAA00217 and manufactured by Medartis 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.

Free DatabasePowered by Pure Global AISFDA Official DataClass IIa