Saudi Arabia SFDA registration ME0000009019SFDAA01233
PERI-LOC VOLAR DISTAL RADIUS LOCKING PLATE
Saudi Arabia·Medical Device·Smith & Nephew Inc.·3ActiveProduct information
A nonbioabsorbable noncustomized firm implantable sheet intended to stabilize a fractured ortho
Device classification
- Risk Class
- 3
- Product Category
- Medical Device
- Product Type
- 1
Registration information
- Registration ID
- ME0000009019SFDAA01233
- Authorization ID
- MDMA-2-2024-3514
- Status
- Active
- Expire Date
- December 15, 2027
Manufacturer
- Manufacturer Name
- Smith & Nephew Inc.
Model information
- Model ID(s)
- 71803110,71803112,71803114,71803116,71803118,71803120,71803122,71803126,71803128,71803124
Product accessories
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About this record
Access comprehensive regulatory information for PERI-LOC VOLAR DISTAL RADIUS LOCKING PLATE in the Saudi Arabia medical device market through Pure Global AI's free database. This 3 device is registered with Saudi Arabia SFDA under registration number ME0000009019SFDAA01233 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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