Cervios - SFDA Registration ME0000000735SFDAA00009
Access comprehensive regulatory information for Cervios 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 ME0000000735SFDAA00009 and manufactured by Synthes 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.
Cage system for interbody fusion in the cervical spine
The device is intended for: Cervical pathologies for which segmental arthrodesis is indicated: – Ruptured and herniated discs – Degenerative disc diseases and instabilities – Pseudarthrosis or failed spondylodesis
[{'tradeName': 'Cancellous Bone Impactor f/Cervios', 'description': None, 'gmdn': '32856'}, {'tradeName': 'Cervios Trial Implant', 'description': None, 'gmdn': '44788'}, {'tradeName': 'Packing Block f/Cervios', 'description': None, 'gmdn': '47743'}]