ProGuide™ DC01453227/A

GUDID 10884450029128

Merit Medical Systems, Inc.

Double-lumen haemodialysis catheter, implantable
Primary Device ID10884450029128
NIH Device Record Key150caa26-8c1b-4aae-a43d-81e8d9e4f584
Commercial Distribution StatusIn Commercial Distribution
Brand NameProGuide™
Version Model Number00884450029121
Catalog NumberDC01453227/A
Company DUNS184763290
Company NameMerit Medical Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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 Perscriptionfalse
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 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 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
GS100884450029121 [Primary]
GS110884450029128 [Package]
Contains: 00884450029121
Package: [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MSDCatheter, hemodialysis, implanted

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-31

On-Brand Devices [ProGuide™]

1088445012002300884450120026
1088445011734400884450117347
1088445009883400884450098837
1088445009641000884450096413
1088445008492900884450084922
1088445008490500884450084908
1088445008282600884450082829
1088445007587300884450075876
1088445007375600884450073759
1088445006886800884450068861
1088445006884400884450068847
1088445006883700884450068830
1088445006882000884450068823
1088445006208800884450062081
1088445006207100884450062074
1088445005726800884450057261
1088445005718300884450057186
1088445005688900884450056882
1088445005666700884450056660
1088445005665000884450056653
1088445005655100884450056554
1088445005612400884450056127
1088445005595000884450055953
1088445005594300884450055946
1088445005593600884450055939
1088445005592900884450055922
1088445005591200884450055915
1088445002973900884450029732
1088445002912800884450029121
1088445002788900884450027882
1088445002787200884450027875
1088445002785800884450027851
1088445002542700884450025420
1088445002342300884450023426
1088445002261700884450022610
1088445001920400884450019207
1088445001253300884450012536
1088445069719800884450697191
1088445069712900884450697122
1088445069722800884450697221
1088445069723500884450697238
1088445069792100884450697924
1088445069791400884450697917
1088445069789100884450697894
1088445069717400884450697177
1088445069790700884450697900
1088445069794500884450697948
1088445069726600884450697269
10884450697259B
10884450827250D

Trademark Results [ProGuide]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROGUIDE
PROGUIDE
86516024 4862246 Live/Registered
Merit Medical Systems, Inc.
2015-01-27
PROGUIDE
PROGUIDE
76620214 not registered Dead/Abandoned
Datascope Trademark Corp.
2004-11-12
PROGUIDE
PROGUIDE
76375494 2807842 Dead/Cancelled
T J SMITH & NEPHEW LMITED
2002-02-26
PROGUIDE
PROGUIDE
75484907 2382190 Live/Registered
PHASES INTERNATIONAL, LTD.
1998-05-14
PROGUIDE
PROGUIDE
74039270 1712612 Dead/Cancelled
Computer Aided Service, Inc.
1990-03-15

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