Saudi Arabia SFDA registration ME0000001920SFDAA00131
Zimmer Natural Nail System, 4.0 mm Diameter, Cortical Screw, White-Partially Threaded
Saudi Arabia·Medical Device·Zimmer Inc.·Class IIbActiveProduct information
Temporary Fracture Fixation Implantable Devices
Product use
Is intended for temporary fracture fixation and stabilization of the bone.
Indications for the Tibial nails include the following in the tibia:
• Compound and simple shaft fractures
• Proximal, metaphyseal and distal shaft fractures
• Segmental fractures
• Comminuted fractures
• Fractures involving osteopenic and osteoporotic bone
• Pathological fractures
• Fractures with bone loss
• Pseudoarthrosis, non-union, mal-union and delayed union
• Periprosthetic fractures
• Surgically created defects such as osteotomies
When this device is implanted using a Suprapatella surgical approach, all of the above indications apply with the
exception of Periprosthetic Fractures.
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000001920SFDAA00131
- Authorization ID
- GHTF-2018-0699
- Status
- Active
- Expire Date
- December 31, 2022
Manufacturer
- Manufacturer Name
- Zimmer Inc.
Model information
- Model ID(s)
- 47-2483-020-40 47-2483-022-40 47-2483-025-40 47-2483-027-40 47-2483-030-40 47-2483-032-40 47-2483-035-40 47-2483-037-40 47-2483-040-40 47-2483-042-40 47-2483-045-40 47-2483-047-40 47-2483-050-40 47-2483-052-40 47-2483-055-40 47-2483-057-40 47-2483-060-40 47-2483-065-40 47-2483-070-40 47-2483-075-40 47-2483-080-40 47-2483-085-40 47-2483-090-40 47-2483-095-40 47-2483-100-40
Product accessories
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About this record
Access comprehensive regulatory information for Zimmer Natural Nail System, 4.0 mm Diameter, Cortical Screw, White-Partially Threaded 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 ME0000001920SFDAA00131 and manufactured by Zimmer 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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb