WRAPSODY® WRAP-L07125

GUDID 00884450845448

Merit Medical Systems, Inc.

Central/peripheral venous endovascular stent-graft

• Primary Device ID: 00884450845448
• NIH Device Record Key: 3160c692-88bd-4d23-a599-c66cf3aefc34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WRAPSODY®
• Version Model Number: A
• Catalog Number: WRAP-L07125
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450845448 [Primary]

FDA Product Code

• PFV: System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment

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: 2025-01-23
• Device Publish Date: 2025-01-15

On-Brand Devices [WRAPSODY®]

• 00884450845875: A
• 00884450845578: A
• 00884450845493: A
• 00884450845936: A
• 00884450845837: A
• 00884450845745: A
• 00884450845592: A
• 00884450845585: A
• 00884450845509: A
• 00884450845448: A