Saudi Arabia SFDA registration ME0000001914SFDAA00080
NCB Periprosthetic Femur Plate
Saudi Arabia·MD·Zimmer GmbH·Class IIbActiveProduct information
Implantable devices made of Titanium alloy long-term surgically invasive
Product use
These implants consist of Proximal Femur plates, Distal Femur plates, and Curved Femur Shaft plates used for the treatment of femur fractures, including Periprosthetic fractures.
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000001914SFDAA00080
- Authorization ID
- GHTF-2018-0735
- Status
- Active
- Expire Date
- July 31, 2023
Manufacturer
- Manufacturer Name
- Zimmer GmbH
Model information
- Model ID(s)
- 02.02263.009 02.02263.012 02.02263.015 02.02263.018 02.02263.021 02.02263.109 02.02263.112 02.02263.115 02.02263.118 02.02263.121 02.02264.009 02.02264.012 02.02264.015 02.02264.018 02.02264.021 02.02264.109 02.02264.112 02.02264.115 02.02264.118 02.02264.121
Product accessories
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About this record
Access comprehensive regulatory information for NCB Periprosthetic Femur Plate 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 ME0000001914SFDAA00080 and manufactured by Zimmer GmbH.
This page provides complete registration details including product category (MD), 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