Squirt®

GUDID 10884450045913

Merit Medical Systems, Inc.

Peripheral vascular infusion catheter

• Primary Device ID: 10884450045913
• NIH Device Record Key: 07652191-e824-425f-8bb2-cc06ff461f6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Squirt®
• Version Model Number: 00884450045916
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450045916 [Primary]
GS1	10884450045913 [Package]; Contains: 00884450045916; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• KRA: Catheter, continuous flush
• QEY: Mechanical Thrombolysis Catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-09
• Device Publish Date: 2016-09-24

On-Brand Devices [Squirt®]

• 10884450045913: 00884450045916
• 10884450830502: A