Saudi Arabia SFDA registration ME0000003446SFDAA00012
ANKYLOS® Conical Reamer
Product 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
- ME0000003446SFDAA00012
- Authorization ID
- GHTF-2019-1988
- Status
- Active
- Expire Date
- August 01, 2019
Manufacturer
- Manufacturer Name
- DENTSPLY Implants Manufacturing GmbH
Model information
- Model ID(s)
- 31037185 31037188 31037190 31037200 31037202 31037205 31037208 31037210 31037220 31037230
Product accessories
[]
About this record
Access comprehensive regulatory information for ANKYLOS® Conical Reamer 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 ME0000003446SFDAA00012 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