RELIANCE 4-FRONT™

GUDID 00802526592805

Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead

BOSTON SCIENTIFIC CORPORATION

Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead
Primary Device ID00802526592805
NIH Device Record Key2578c3b8-0b44-4b13-9c25-6b13ffbcf987
Commercial Distribution StatusIn Commercial Distribution
Brand NameRELIANCE 4-FRONT™
Version Model Number0663
Company DUNS106295384
Company NameBOSTON SCIENTIFIC CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100802526592805 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NVYPermanent defibrillator electrodes

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-10-09
Device Publish Date2018-08-25

On-Brand Devices [RELIANCE 4-FRONT™]

00802526592874Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592867Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592850Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592843Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592836Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592829Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592812Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526592805Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526497001Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526496981Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526496967Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead
00802526496868Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead

Trademark Results [RELIANCE 4-FRONT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RELIANCE 4-FRONT
RELIANCE 4-FRONT
87599526 5885914 Live/Registered
Cardiac Pacemakers, Inc.
2017-09-07
RELIANCE 4-FRONT
RELIANCE 4-FRONT
86233013 not registered Dead/Abandoned
Cardiac Pacemakers, Inc.
2014-03-26
RELIANCE 4-FRONT
RELIANCE 4-FRONT
76704342 not registered Dead/Abandoned
Cardiac Pacemakers, Inc.
2010-09-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.