NovaCath™ 240750

GUDID 10887709090436

Peripheral intravenous cannula

Primary Device ID	10887709090436
NIH Device Record Key	5d766c18-c5f9-4d1e-bbfd-111fdeb4e6ed
Commercial Distribution Status	In Commercial Distribution
Brand Name	NovaCath™
Version Model Number	240750
Catalog Number	240750
Company DUNS	118380146
Company Name	ICU MEDICAL, INC.
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	true
Serial Number	false
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

Device Issuing Agency	Device ID
GS1	00887709090439 [Primary]
GS1	10887709090436 [Package] Contains: 00887709090439 Package: CS [100 Units] In Commercial Distribution

FOZ	Catheter, intravascular, therapeutic, short-term less than 30 days

Steralize Prior To Use	false
Device Is Sterile	true

10887709121581	NovaCath Integrated IV Catheter System 22G x 0.75in
10887709090436	NovaCath Integrated IV Catheter System 24G x 0.75in
10887709090368	NovaCath Integrated IV Catheter System 22G x 1.00in

Mark Image Registration \| Serial	Company Trademark Application Date
NOVACATH 85099004 4432814 Live/Registered	Tangent Medical Technologies, Inc. 2010-08-03