Prelude Wave™ WAV5F11021SSC-F

GUDID 20884450068872

Merit Medical Systems, Inc.

Vascular catheter introduction set, nonimplantable

• Primary Device ID: 20884450068872
• NIH Device Record Key: 737f2fa2-8e08-4ab7-b7d9-148db2c9f912
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prelude Wave™
• Version Model Number: Initial Release
• Catalog Number: WAV5F11021SSC-F
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 5
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450068878 [Unit of Use]
GS1	10884450068875 [Primary]
GS1	20884450068872 [Package]; Contains: 10884450068875; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DYB: Introducer, 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: 2025-08-04
• Device Publish Date: 2025-07-26

On-Brand Devices [Prelude Wave™]

• 20884450072206: Initial Release
• 20884450071131: Initial Release
• 20884450068872: Initial Release
• 20884450065444: Initial Release