Finale® FCD200/A

GUDID 20884450034358

Merit Medical Systems, Inc.

Vascular compressor, external

• Primary Device ID: 20884450034358
• NIH Device Record Key: 15b10c36-6023-49d2-a771-da7e6bc0c2a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finale®
• Version Model Number: 00884450034354
• Catalog Number: FCD200/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00884450034354 [Primary]
GS1	10884450034351 [Package]; Contains: 00884450034354; Package: [10 Units]; In Commercial Distribution
GS1	20884450034358 [Package]; Contains: 10884450034351; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• GAX: TOURNIQUET, NONPNEUMATIC

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: 2018-10-22
• Device Publish Date: 2018-09-21

On-Brand Devices [Finale®]

• 20884450034358: 00884450034354
• 20884450034341: 00884450034347