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PERI-LOC SELF TAPPING CORTEX SCREW - SFDA Registration ME0000009019SFDAA01230

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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3
ME0000009019SFDAA01230
PERI-LOC SELF TAPPING CORTEX SCREW
SFDA Registration: ME0000009019SFDAA01230
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Product 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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