Saudi Arabia SFDA registration ME0000003446SFDAA00016
ANKYLOS® Tri-Spade Drill
Saudi Arabia·MD·DENTSPLY Implants Manufacturing GmbH·Class IIaActiveProduct information
Machine driven rotating surgical instruments Surgical Drill.
Product use
Machine driven rotating surgical instruments & Preparing the implant site with a handpiece or contra-angle
Device classification
- Risk Class
- Class IIa
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000003446SFDAA00016
- Authorization ID
- GHTF-2019-1988
- Status
- Active
- Expire Date
- August 01, 2019
Manufacturer
- Manufacturer Name
- DENTSPLY Implants Manufacturing GmbH
Model information
- Model ID(s)
- 31037324 31037325 31037330 31037340 31037344 31037345 31037350 31037360 31037364 31037365 31037370 31037380
Product accessories
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About this record
Access comprehensive regulatory information for ANKYLOS® Tri-Spade 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 ME0000003446SFDAA00016 and manufactured by DENTSPLY Implants Manufacturing GmbH.
This page provides complete registration details including product category (MD), 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