Saudi Arabia SFDA registration ME0000009019SFDAA01230
PERI-LOC SELF TAPPING CORTEX SCREW
Saudi Arabia·Medical Device·Smith & Nephew Inc.·3ActiveProduct information
A small sterile threaded rod with a slotted head used for internal orthopaedic fracture fixation
Device classification
- Risk Class
- 3
- Product Category
- Medical Device
- Product Type
- 1
Registration information
- Registration ID
- ME0000009019SFDAA01230
- Authorization ID
- MDMA-2-2024-3514
- Status
- Active
- Expire Date
- December 15, 2027
Manufacturer
- Manufacturer Name
- Smith & Nephew Inc.
Model information
- Model ID(s)
- 71802510,71802512,71802530,71802514,71802516,71802518,71802520,71802522,71802524,71802526,71802528
Product accessories
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About this record
Access comprehensive regulatory information for PERI-LOC SELF TAPPING CORTEX SCREW 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 ME0000009019SFDAA01230 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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