GuideRight™ 404612

GUDID 15414734010631

Guidewires

ST. JUDE MEDICAL, INC.

Cardiac/peripheral vascular guidewire, single-use
Primary Device ID15414734010631
NIH Device Record Key9996cbdc-4740-4deb-bba6-f42388abeb77
Commercial Distribution Discontinuation2018-06-29
Commercial Distribution StatusNot in Commercial Distribution
Brand NameGuideRight™
Version Model Number404612
Catalog Number404612
Company DUNS149818952
Company NameST. JUDE MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com

Device Dimensions

Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter
Outer Diameter0.97 Millimeter

Operating and Storage Conditions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS105414734010634 [Primary]
GS115414734010631 [Package]
Contains: 05414734010634
Package: [5 Units]
Discontinued: 2018-06-29
Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQXWIRE, GUIDE, CATHETER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-19
Device Publish Date2015-06-23

On-Brand Devices [GuideRight™]

15415067009262405022
15415067009255405020
15415067009248405016
15414734054901Guidewires
15414734054895Guidewires
15414734054871Guidewires
15414734054857Guidewires
15414734054833Guidewires
15414734054819Guidewires
15414734054796Guidewires
15414734054109404586
15414734026632Guidewires
15414734013717Guidewires
15414734013700Guidewires
15414734013670405050
15414734013656Guidewires
15414734013632Guidewires
15414734013618Guidewires
15414734013601Guidewires
15414734013571Guidewires
15414734013557404968
15414734013533Guidewires
15414734013519404878
15414734013496404877
15414734013472404876
15414734013458404874
15414734013434Guidewires
15414734013410Guidewires
15414734013397404843
15414734013380404841
15414734013359Guidewires
15414734013342404582
15414734013311404581
15414734013298404580
15414734013274404578
15414734013250404574
15414734013236Guidewires
15414734013212Guidewires
15414734013199Guidewires
15414734013175404560
15414734013151404557
15414734013137404555
15414734013113Guidewires
15414734013090Guidewires
15414734013076404552
15414734013052Guidewires
15414734010716Guidewires
15414734010693Guidewires
15414734010679Guidewires
15414734010655Guidewires

Trademark Results [GuideRight]

Mark Image

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

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