VeriFLEX™ H7493893516300

GUDID 08714729396048

Coronary Stent System

BOSTON SCIENTIFIC CORPORATION

Coronary angioplasty balloon catheter, basic
Primary Device ID08714729396048
NIH Device Record Keyebf70e06-b140-43ae-bfea-a816cd880eb4
Commercial Distribution Discontinuation2018-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameVeriFLEX™
Version Model NumberH7493893516300
Catalog NumberH7493893516300
Company DUNS021717889
Company NameBOSTON SCIENTIFIC CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS108714729396048 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAFSTENT, CORONARY

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-06-23
Device Publish Date2014-09-24

On-Brand Devices [VeriFLEX™]

08714729471417Coronary Stent System
08714729471400Coronary Stent System
08714729471394Coronary Stent System
08714729471387Coronary Stent System
08714729396383Coronary Stent System
08714729396376Coronary Stent System
08714729396369Coronary Stent System
08714729396352Coronary Stent System
08714729396321Coronary Stent System
08714729396314Coronary Stent System
08714729396307Coronary Stent System
08714729396291Coronary Stent System
08714729396284Coronary Stent System
08714729396277Coronary Stent System
08714729396260Coronary Stent System
08714729396253Coronary Stent System
08714729396246Coronary Stent System
08714729396239Coronary Stent System
08714729396222Coronary Stent System
08714729396215Coronary Stent System
08714729396208Coronary Stent System
08714729396192Coronary Stent System
08714729396161Coronary Stent System
08714729396154Coronary Stent System
08714729396147Coronary Stent System
08714729396130Coronary Stent System
08714729396123Coronary Stent System
08714729396116Coronary Stent System
08714729396086Coronary Stent System
08714729396079Coronary Stent System
08714729396062Coronary Stent System
08714729396055Coronary Stent System
08714729396048Coronary Stent System
08714729396031Coronary Stent System
08714729396000Coronary Stent System
08714729395997Coronary Stent System
08714729395980Coronary Stent System
08714729395973Coronary Stent System
08714729395966Coronary Stent System
08714729395959Coronary Stent System
08714729395928Coronary Stent System
08714729395911Coronary Stent System
08714729395904Coronary Stent System
08714729395898Coronary Stent System
08714729395867Coronary Stent System
08714729395850Coronary Stent System
08714729395843Coronary Stent System
08714729395836Coronary Stent System
08714729395829Coronary Stent System
08714729395812Coronary Stent System

Trademark Results [VeriFLEX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERIFLEX
VERIFLEX
97501375 not registered Live/Pending
OMNOVA Solutions Inc.
2022-07-13
VERIFLEX
VERIFLEX
87619282 5657037 Live/Registered
Arrowhead Healthcare Supply, LLC
2017-09-22
VERIFLEX
VERIFLEX
78551381 3050469 Dead/Cancelled
Cornerstone Research Group, Inc.
2005-01-21
VERIFLEX
VERIFLEX
78472737 3745425 Live/Registered
BOSTON SCIENTIFIC SCIMED, INC.
2004-08-24
VERIFLEX
VERIFLEX
78190691 not registered Dead/Abandoned
Advanced Medical Optics, Inc.
2002-12-03
VERIFLEX
VERIFLEX
78026837 not registered Dead/Abandoned
Hewlett-Packard Company
2000-09-20
VERIFLEX
VERIFLEX
77444937 3530862 Dead/Cancelled
ABBOTT MEDICAL OPTICS INC.
2008-04-10
VERIFLEX
VERIFLEX
76600432 3077221 Dead/Cancelled
PRINTING TECHNOLOGY SERVICES, INC.
2004-07-02
VERIFLEX
VERIFLEX
73467836 1316758 Dead/Cancelled
Nuson Trading & Engineering ApS
1984-02-29
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