Evolution® RL LR-EVN-11.0-RL

GUDID 10884450441616

Merit Medical Systems, Inc.

Fascial tissue dilator, single-use

• Primary Device ID: 10884450441616
• NIH Device Record Key: de111c9e-e064-4084-ac1a-1510c7b4db05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Evolution® RL
• Version Model Number: B
• Catalog Number: LR-EVN-11.0-RL
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450441619 [Primary]
GS1	10884450441616 [Package]; Contains: 00884450441619; Package: [7 Units]; In Commercial Distribution

FDA Product Code

• DRE: Dilator, Vessel, For Percutaneous Catheterization

Sterilization

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

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

[10884450441616]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-19
• Device Publish Date: 2026-03-11

On-Brand Devices [Evolution® RL]

• 10884450441623: B
• 10884450441753: B
• 10884450441746: B
• 10884450441616: B