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XRL Medium - SFDA Registration ME0000000735SFDAA00566

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.

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Class IIb
ME0000000735SFDAA00566
XRL Medium
SFDA Registration: ME0000000735SFDAA00566
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Product 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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