Saudi Arabia SFDA registration ME0000009019SFDAA00171
Legion PS XLPE High flexion Articular Insert
Saudi Arabia·Medical Device·Smith & Nephew Inc.·Class IIActiveProduct information
Posterior stabilized knee Surgical instruments
Product use
Device used for reconstructive knee surgery
Device classification
- Risk Class
- Class II
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000009019SFDAA00171
- Authorization ID
- GHTF-2020-1453
- Status
- Active
- Expire Date
- July 03, 2023
Manufacturer
- Manufacturer Name
- Smith & Nephew Inc.
Model information
- Model ID(s)
- 71453201 71453202 71453203 71453204 71453205 71453206 71453207 71453211 71453212 71453213 71453214 71453215 71453216 71453217 71453222 71453223 71453224 71453225 71453226 71453227 71453231 71453232 71453233 71453234 71453235 71453236 71453237
Product accessories
[]
About this record
Access comprehensive regulatory information for Legion PS XLPE High flexion Articular Insert in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000009019SFDAA00171 and manufactured by Smith & Nephew Inc..
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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