Guide Camlog SL Implant - SFDA Registration ME0000001463SFDAA00059
Access comprehensive regulatory information for Guide Camlog SL Implant in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000001463SFDAA00059 and manufactured by ALTATEC GmbH.
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.
device connected to the dental implant and aids in prosthetic rehabilitation
The components of the Guide System are used for template-guided preparation of the implant bed and for insertion of Guide System SCREW-LINE Implants, Promote® plus, in a partially or fully edentulous maxilla and mandible. In order to be able to use the Guide System, the practice/ laboratory must be equipped with a suitable 3D planning system (also to design the respective drilling template) and, where necessary, the appropriate guiding sleeve positioning system.
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