Novatome™ SU102-50

GUDID 10884450392796

Merit Medical Systems, Inc.

Endomyocardial biopsy forceps, single-use

• Primary Device ID: 10884450392796
• NIH Device Record Key: a1a2274a-5a1c-4880-a592-7e91aff8f1cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Novatome™
• Version Model Number: C
• Catalog Number: SU102-50
• 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	00884450392799 [Primary]
GS1	10884450392796 [Package]; Contains: 00884450392799; Package: [60 Units]; In Commercial Distribution

FDA Product Code

• DWZ: DEVICE, BIOPSY, ENDOMYOCARDIAL

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: 2026-02-23
• Device Publish Date: 2026-02-14

On-Brand Devices [Novatome™]

• 10884450392796: C
• 10884450392840: C
• 10884450392826: C