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NCB Periprosthetic Femur Plate - SFDA Registration ME0000001914SFDAA00080

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.

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Class IIb
ME0000001914SFDAA00080
NCB Periprosthetic Femur Plate
SFDA Registration: ME0000001914SFDAA00080
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Product 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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