Saudi Arabia SFDA registration ME0000000735SFDAA00009
Cervios
Saudi Arabia·Medical Device·Synthes GmbH·Class IIbActiveProduct information
Cage system for interbody fusion in the cervical spine
Product use
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
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000735SFDAA00009
- Authorization ID
- GHTF-2015-0324
- Status
- Active
- Expire Date
- December 22, 2017
Manufacturer
- Manufacturer Name
- Synthes GmbH
Model information
- Model ID(s)
- 889.936S 889.931S 889.932S 889.933S 889.934S 889.935S 889.926S 889.921S 889.922S 889.923S 889.924S 889.925S
Product accessories
[{'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'}]
About this record
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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb