SplashWire™ MSWSTDS25180

GUDID 10884450529482

Merit Medical Systems, Inc.

Peripheral vascular guidewire, manual

• Primary Device ID: 10884450529482
• NIH Device Record Key: f5571635-ad5c-4986-813a-dae9175b52e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SplashWire™
• Version Model Number: Initial Release
• Catalog Number: MSWSTDS25180
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450529485 [Primary]
GS1	10884450529482 [Package]; Contains: 00884450529485; Package: [5 Units]; In Commercial Distribution
GS1	20884450529489 [Package]; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• DQX: Wire, guide, catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-10
• Device Publish Date: 2025-12-02

On-Brand Devices [SplashWire™]

• 20884450529663: 00884450529669
• 10884450529642: 00884450529645
• 20884450529564: 00884450529560
• 10884450529444: 00884450529447
• 10884450529352: 00884450529355
• 20884450529311: 00884450529317
• 10884450529758: 00884450529751
• 10884450529680: 00884450529683
• 10884450529598: 00884450529591
• 10884450529673: 00884450529676
• 20884450529519: 00884450529515
• 10884450529697: 00884450529690
• 10884450529741: 00884450529744
• 10884450529789: 00884450529782
• 20884450529502: 00884450529508
• 20884450529380: 00884450529386
• 20884450529366: 00884450529362
• 20884450529656: 00884450529652
• 10884450529611: 00884450529614
• 10884450529550: 00884450529553
• 10884450529604: 00884450529607
• 10884450529437: 00884450529430
• 10884450529772: 00884450529775
• 10884450529574: 00884450529577
• 20884450529540: 00884450529546
• 20884450529526: 00884450529522
• 10884450529406: 00884450529409
• 10884450529468: 00884450529461
• 20884450529274: 00884450529270
• 10884450529819: 00884450529812
• 10884450529796: 00884450529799
• 10884450529833: 00884450529836
• 10884450529734: 00884450529737
• 10884450529840: 00884450529843
• 20884450529632: 00884450529638
• 10884450529857: 00884450529850
• 20884450529762: 00884450529768
• 20884450529267: Initial Release
• 20884450529472: Initial Release
• 10884450529482: Initial Release