Saudi Arabia SFDA registration ME0000000735SFDAA00566
XRL Medium
Saudi Arabia·Medical Device·Synthes GmbH·Class IIbActiveProduct information
Implants for stabilizing the anterior thoracic and lumbar spine
Product use
The device is intended for:
Replacement for injured vertebral bodies to stabilize the anterior thoracic and lumbar spine (Th3-L5)
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000735SFDAA00566
- Authorization ID
- GHTF-2015-1465
- Status
- Active
- Expire Date
- December 22, 2017
Manufacturer
- Manufacturer Name
- Synthes GmbH
Model information
- Model ID(s)
- 08.807.201S 08.807.202S 08.807.203S 08.807.204S 08.807.205S 08.807.206S 08.807.207S 08.807.208S 08.807.209S 08.807.210S 08.807.211S 08.807.212S 08.807.213S 08.807.214S 08.807.215S
Product accessories
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About this record
Access comprehensive regulatory information for XRL Medium 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 ME0000000735SFDAA00566 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