Performa® 7240-20/B

GUDID 10884450001209

Merit Medical Systems, Inc.

Angiographic catheter, single-use
Primary Device ID10884450001209
NIH Device Record Keyb973d402-3b81-492f-b748-778556907c9d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePerforma®
Version Model Number00884450001202
Catalog Number7240-20/B
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 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 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 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
GS100884450001202 [Primary]
GS110884450001209 [Package]
Contains: 00884450001202
Package: [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC

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 Date2016-09-24

On-Brand Devices [Performa®]

1088445040858900884450408582
1088445040857200884450408575
1088445039474500884450394748
1088445039472100884450394724
1088445038341100884450383414
1088445038340400884450383407
1088445036311600884450363119
1088445036294200884450362945
1088445036284300884450362846
1088445036283600884450362839
1088445036282900884450362822
1088445036280500884450362808
1088445036264500884450362648
1088445036263800884450362631
1088445036262100884450362624
1088445036257700884450362570
1088445036256000884450362563
1088445036255300884450362556
1088445036254600884450362549
1088445036222500884450362228
1088445036221800884450362211
1088445036219500884450362198
1088445036218800884450362181
1088445036216400884450362167
1088445036215700884450362150
1088445036210200884450362105
1088445036209600884450362099
1088445036208900884450362082
1088445036206500884450362068
1088445036204100884450362044
1088445036202700884450362020
1088445036200300884450362006
1088445036093100884450360934
1088445035887700884450358870
1088445035667500884450356678
1088445035660600884450356609
1088445035659000884450356593
1088445035658300884450356586
1088445035657600884450356579
1088445035656900884450356562
1088445035655200884450356555
1088445032075100884450320754
1088445032074400884450320747
1088445032073700884450320730
1088445032072000884450320723
1088445031479800884450314791
1088445030960200884450309605
1088445030700400884450307007
1088445030697700884450306970
1088445030682300884450306826

Trademark Results [Performa]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERFORMA
PERFORMA
98355199 not registered Live/Pending
Colson Group USA, LLC
2024-01-12
PERFORMA
PERFORMA
98128394 not registered Live/Pending
Gerdau Macsteel, Inc.
2023-08-11
PERFORMA
PERFORMA
90723564 not registered Live/Pending
ARCESIUM LLC
2021-05-20
PERFORMA
PERFORMA
88734959 not registered Live/Pending
Quadratec, Inc.
2019-12-20
PERFORMA
PERFORMA
88663369 not registered Live/Pending
Reece Australia Pty Ltd
2019-10-22
PERFORMA
PERFORMA
88354438 not registered Live/Pending
ENERGIZER AUTO, INC.
2019-03-25
PERFORMA
PERFORMA
88095900 not registered Dead/Abandoned
AS IP Holdco, LLC
2018-08-28
PERFORMA
PERFORMA
88004914 5679143 Live/Registered
Perfoma Limited (US) LLC
2018-06-18
PERFORMA
PERFORMA
87570253 not registered Live/Pending
Cyrus Creations LLC
2017-08-15
PERFORMA
PERFORMA
87551203 not registered Live/Pending
1535674 Alberta, Inc.
2017-08-01
PERFORMA
PERFORMA
87457413 not registered Dead/Abandoned
Vytalyx Inc
2017-05-19
PERFORMA
PERFORMA
87379635 5461970 Live/Registered
Performance Health Holdings, Inc.
2017-03-21

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