HLS NOETOS REVISION

GUDID 03700386911682

Knee femur stem prosthesis

Primary Device ID	03700386911682
NIH Device Record Key	a2b37421-317f-4226-b042-f272858d9745
Commercial Distribution Discontinuation	2017-11-30
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	HLS NOETOS REVISION
Version Model Number	GDF513
Company DUNS	260324876
Company Name	TORNIER
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Phone	+330476613500
Email	order@tornier.com

Outer Diameter

14 Millimeter

Device Issuing Agency	Device ID
GS1	03700386911682 [Primary]

JWH	PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Steralize Prior To Use	false
Device Is Sterile	true