Tru-Cut® 2N2702X/B

GUDID 20884450443020

Merit Medical Systems, Inc.

Soft-tissue biopsy procedure kit, non-medicated

• Primary Device ID: 20884450443020
• NIH Device Record Key: cba272b5-b93e-4eb3-99e3-6b6c3b26ac6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tru-Cut®
• Version Model Number: 10884450443023
• Catalog Number: 2N2702X/B
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 10
• 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: true
• 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	00884450443026 [Unit of Use]
GS1	10884450443023 [Primary]
GS1	20884450443020 [Package]; Contains: 10884450443023; Package: [2 Units]; In Commercial Distribution

FDA Product Code

• KNW: INSTRUMENT, BIOPSY

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: 2020-06-03
• Device Publish Date: 2020-05-26

On-Brand Devices [Tru-Cut®]

• 20884450443020: 10884450443023
• 20884450443044: 10884450443047
• 20884450443013: 10884450443016
• 20884450394650: 10884450394653
• 20884450394643: 10884450394646
• 20884450443075: 10884450443078
• 20884450394681: 10884450394684
• 20884450443068: 10884450443061
• 20884450831520: C
• 20884450831513: C