Merit Pursue™ 28HC1711045/A

GUDID 10884450358488

Merit Medical Systems, Inc.

Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter

• Primary Device ID: 10884450358488
• NIH Device Record Key: ee8a7e05-99c9-45c8-bdc3-15b00c04de74
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merit Pursue™
• Version Model Number: 00884450358481
• Catalog Number: 28HC1711045/A
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450358481 [Primary]
GS1	10884450358488 [Package]; Contains: 00884450358481; Package: [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173548

FDA Product Code

• DQY: Catheter, percutaneous

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: 2020-02-11
• Device Publish Date: 2020-02-03

On-Brand Devices [Merit Pursue™]

• 10884450358747: 00884450358740
• 10884450358730: 00884450358733
• 10884450358723: 00884450358726
• 10884450358716: 00884450358719
• 10884450358686: 00884450358689
• 10884450358679: 00884450358672
• 10884450358662: 00884450358665
• 10884450358563: 00884450358566
• 10884450358556: 00884450358559
• 10884450358549: 00884450358542
• 10884450358532: 00884450358535
• 10884450358525: 00884450358528
• 10884450358495: 00884450358498
• 10884450358501: 00884450358504
• 10884450357719: 00884450357712
• 10884450357672: 00884450357675
• 10884450357580: 00884450357583
• 10884450357542: 00884450357545
• 10884450357504: 00884450357507
• 10884450358488: 00884450358481
• 10884450357733: 00884450357736