Merit Pursue™ 29HC2015045/A

GUDID 10884450358723

Merit Medical Systems, Inc.

Vascular microcatheter

• Primary Device ID: 10884450358723
• NIH Device Record Key: d258d6eb-b198-4129-8237-810b6b1add97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merit Pursue™
• Version Model Number: 00884450358726
• Catalog Number: 29HC2015045/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 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	00884450358726 [Primary]
GS1	10884450358723 [Package]; Contains: 00884450358726; 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-03-21
• Device Publish Date: 2018-07-09

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