Pure Global

Zimmer Natural Nail System, 6.0 mm Diameter Cancellous Screw - Black - Fixed Angle - SFDA Registration ME0000001920SFDAA00137

Access comprehensive regulatory information for Zimmer Natural Nail System, 6.0 mm Diameter Cancellous Screw - Black - Fixed Angle 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 ME0000001920SFDAA00137 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 Database
Powered by Pure Global AI
SFDA Official Data
Class IIb
ME0000001920SFDAA00137
Zimmer Natural Nail System, 6.0 mm Diameter Cancellous Screw - Black - Fixed Angle
SFDA Registration: ME0000001920SFDAA00137
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product 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: โ€ข Compound and simple shaft fractures โ€ข Proximal, metaphyseal and distal shaft fractures โ€ข Segmental fractures โ€ข Comminuted fractures โ€ข Fractures involving osteopenic and osteoporotic bone โ€ข Pathological fractures โ€ข Fractures with bone loss โ€ข Pseudoarthrosis, non-union, mal-union and delayed union โ€ข Periprosthetic fractures โ€ข 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
ME0000001920SFDAA00137
Authorization ID
GHTF-2018-0699
Status
Active
Expire Date
December 31, 2022
Manufacturer
Manufacturer Name
Zimmer Inc.
Model Information
Model ID(s)
47-2484-030-60 47-2484-035-60 47-2484-040-60 47-2484-045-60 47-2484-050-60 47-2484-055-60 47-2484-060-60 47-2484-065-60 47-2484-070-60 47-2484-075-60 47-2484-080-60 47-2484-085-60 47-2484-090-60 47-2484-095-60 47-2484-100-60 47-2484-105-60 47-2484-110-60 47-2484-115-60 47-2484-120-60 47-2484-125-60 47-2484-130-60 47-2484-135-60 47-2484-140-60
Product Accessories

[]