Saudi Arabia SFDA registration ME0000003446SFDAA00008
ANKYLOS® Taper cap Degulor®
Saudi Arabia·MD·DENTSPLY Implants Manufacturing GmbH·Class IIaActiveProduct information
Prosthetic dental implant device Titanium Abutment Cap
Product use
Anchorage of removable dentures
Device classification
- Risk Class
- Class IIa
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000003446SFDAA00008
- Authorization ID
- GHTF-2019-1988
- Status
- Active
- Expire Date
- August 01, 2019
Manufacturer
- Manufacturer Name
- DENTSPLY Implants Manufacturing GmbH
Model information
- Model ID(s)
- 31022198 31022199
Product accessories
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About this record
Access comprehensive regulatory information for ANKYLOS® Taper cap Degulor® 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 ME0000003446SFDAA00008 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