Mistique®

GUDID 10884450012120

Merit Medical Systems, Inc.

Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter

Primary Device ID	10884450012120
NIH Device Record Key	53900239-91bf-4b7c-bee0-12949eef5dce
Commercial Distribution Status	In Commercial Distribution
Brand Name	Mistique®
Version Model Number	00884450012123
Company DUNS	184763290
Company Name	Merit Medical Systems, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Dimensions

Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450012123 [Primary]
GS1	10884450012120 [Package] Contains: 00884450012123 Package: [5 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K974067

FDA Product Code

KRA	Catheter, continuous flush

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	5
Public Version Date	2019-04-09
Device Publish Date	2016-09-24

On-Brand Devices [Mistique®]

10884450012151	00884450012154
10884450012144	00884450012147
10884450012120	00884450012123
10884450012113	00884450012116
10884450012090	00884450012093
10884450012083	00884450012086

Trademark Results [Mistique]

Mark Image Registration \| Serial	Company Trademark Application Date
MISTIQUE 88114314 not registered Live/Pending	East West Import Export, Inc. 2018-09-12
MISTIQUE 87663373 5728891 Live/Registered	Naz 64, Inc. 2017-10-27
MISTIQUE 86070978 4668429 Live/Registered	Unitrex, Inc. 2013-09-20
MISTIQUE 78645425 not registered Dead/Abandoned	The Yankee Candle Company, Inc. 2005-06-07
MISTIQUE 78640884 3097895 Dead/Cancelled	PEARLESSENCE, LTD. 2005-06-01
MISTIQUE 76591185 not registered Dead/Abandoned	PEJU PROVINCE 2004-05-10
MISTIQUE 76274203 2644315 Live/Registered	SOLO CUP OPERATING CORPORATION 2001-06-20
MISTIQUE 75767457 2532684 Live/Registered	Merit Medical Systems, Inc. 1999-08-04
MISTIQUE 75376254 2220335 Dead/Cancelled	Pittsburgh Corning Corporation 1997-10-20
MISTIQUE 74619493 not registered Dead/Abandoned	Land O'Lakes, Inc. 1994-12-02
MISTIQUE 74619492 not registered Dead/Abandoned	Land O'Lakes, Inc. 1994-12-02
MISTIQUE 74083986 1649414 Dead/Cancelled	General Bicycle and Moped Co., Inc. 1990-07-31