GuideRight™ 404876

GUDID 15414734013472

Cardiac/peripheral vascular guidewire, single-use

Primary Device ID	15414734013472
NIH Device Record Key	80394ca7-958d-4b72-98db-f152f0c8eef8
Commercial Distribution Status	In Commercial Distribution
Brand Name	GuideRight™
Version Model Number	404876
Catalog Number	404876
Company DUNS	149818952
Company Name	ST. JUDE 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	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.
Special Storage Condition, Specify	Between 0 and 0 *STORE IN A COOL, DARK, DRY PLACE.

Device Issuing Agency	Device ID
GS1	05414734013475 [Primary]
GS1	15414734013472 [Package] Contains: 05414734013475 Package: [5 Units] In Commercial Distribution

DQX	WIRE, GUIDE, CATHETER

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
GUIDERIGHT 87852320 not registered Live/Pending	GuideRight Assessments, LLC 2018-03-27
GUIDERIGHT 77413917 3772274 Dead/Cancelled	Dreambox Learning Inc. 2008-03-05
GUIDERIGHT 75916824 not registered Dead/Abandoned	Virtual Carrier Network, Inc. 2000-02-10
GUIDERIGHT 75222634 2181424 Dead/Cancelled	Daig Corporation 1997-01-08