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VIPER SYSTEM SINGLE INNER SET SCREW - SFDA Registration ME0000000631SFDAA00047

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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Class IIb
ME0000000631SFDAA00047
VIPER SYSTEM SINGLE INNER SET SCREW
SFDA Registration: ME0000000631SFDAA00047
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Product 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

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