DiamondTOUCH™ IN9403

GUDID 10884450324810

Merit Medical Systems, Inc.

Catheter/overtube balloon inflator, single-use
Primary Device ID10884450324810
NIH Device Record Keyc04b41a6-0379-428a-8c45-7cb851234011
Commercial Distribution StatusIn Commercial Distribution
Brand NameDiamondTOUCH™
Version Model Number00884450324813
Catalog NumberIN9403
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 Identifiers

Device Issuing AgencyDevice ID
GS100884450324813 [Primary]
GS110884450324810 [Package]
Contains: 00884450324813
Package: [5 Units]
In Commercial Distribution
GS120884450324817 [Package]
Package: [2 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXTINJECTOR AND SYRINGE, ANGIOGRAPHIC

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-05-06
Device Publish Date2018-03-29

On-Brand Devices [DiamondTOUCH™]

1088445032481000884450324813
2088445032480000884450324806
1088445032478000884450324783
2088445026490800884450264904
2088445041346700884450413463
1088445040965400884450409657
1088445040964700884450409640

Trademark Results [DiamondTOUCH]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DIAMONDTOUCH
DIAMONDTOUCH
87352328 5630343 Live/Registered
Q.E.P. CO., INC.
2017-02-28

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