Neuroguard IEP® System NG-0740-140-2

GUDID 00851616007613

Peripheral angioplasty balloon catheter, basic

Primary Device ID	00851616007613
NIH Device Record Key	b640ad63-1601-4575-b9a3-5dbc94b30c36
Commercial Distribution Status	In Commercial Distribution
Brand Name	Neuroguard IEP® System
Version Model Number	NG-0740-140-2
Catalog Number	NG-0740-140-2
Company DUNS	048268128
Company Name	Contego Medical, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
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

Device Issuing Agency	Device ID
GS1	00851616007613 [Primary]

NIM	Stent, Carotid

Steralize Prior To Use	false
Device Is Sterile	true

00851616007613	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007606	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007590	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007583	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007651	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007644	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007637	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent
00851616007620	The Neuroguard IEP System consists of three main components: • A self-expanding nitinol stent

Mark Image Registration \| Serial	Company Trademark Application Date
NEUROGUARD IEP 87274946 not registered Live/Pending	Contego Medical, LLC 2016-12-20