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CAMLOG ROOT LINE 2 Implant - SFDA Registration ME0000001463SFDAA00073

Access comprehensive regulatory information for CAMLOG ROOT LINE 2 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 ME0000001463SFDAA00073 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.

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Class IIb
ME0000001463SFDAA00073
CAMLOG ROOT LINE 2 Implant
SFDA Registration: ME0000001463SFDAA00073
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Product Information

device connected to the dental implant and aids in prosthetic rehabilitation

Product Use

ROOT-LINE 2 implants represent root-shaped screw implants in terms of their outer geometry. The implants can be employed as immediate or delayed immediate implants in the bone of the maxilla and mandible. In the case of a one-stage surgical procedure, the implants can be loaded immediately if good primary stability has been achieved and functional loading is appropriate. Abutments are used for the prosthetic restoration with crowns, bridges and full prosthesis for the esthetic oral restoration for partially and fully edentulous patients.

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000001463SFDAA00073
Authorization ID
GHTF-2019-0518
Status
Active
Expire Date
June 29, 2022
Manufacturer
Manufacturer Name
ALTATEC GmbH
Model Information
Model ID(s)
K1032.3311 K1032.3313 K1032.3316 K1032.3811 K1032.3813 K1032.3816 K1032.3809 K1032.4311 K1032.4313 K1032.4316 K1032.4309 K1032.5011 K1032.5013 K1032.5016 K1032.5009 K1032.6011 K1032.6013 K1032.6016 K1032.6009
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