Saudi Arabia SFDA registration ME0000000631SFDAA00047
VIPER SYSTEM SINGLE INNER SET SCREW
Saudi Arabia·MD·Medos International SARL·Class IIbActiveProduct information
Spinal Implant
Product use
The VIPER System is intended to be
used to
provide immobilization and stabilization of spinal segments
in the treatment of acute and chronic instabilities or
deformities of the thoracic, lumbar and sacral spine
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000631SFDAA00047
- Authorization ID
- MDMA-1-2019-4683
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- Medos International SARL
Model information
- Model ID(s)
- 186715000
Product accessories
[]
About this record
Access comprehensive regulatory information for VIPER SYSTEM SINGLE INNER SET SCREW 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 ME0000000631SFDAA00047 and manufactured by Medos International SARL.
This page provides complete registration details including product category (MD), 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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