TRAM®P 501LTCHF-R

GUDID 10884450312459

Merit Medical Systems, Inc.

Stopcock

• Primary Device ID: 10884450312459
• NIH Device Record Key: 5bfc69a2-2839-455f-b248-d398a0a23121
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRAM®P
• Version Model Number: D
• Catalog Number: 501LTCHF-R
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450312452 [Primary]
GS1	10884450312459 [Package]; Contains: 00884450312452; Package: [10 Units]; In Commercial Distribution
GS1	20884450312456 [Package]; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DTL: Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass

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: 2025-12-31
• Device Publish Date: 2025-12-23

On-Brand Devices [TRAM®P]

• 20884450312326: 00884450312322
• 10884450312305: 00884450312308
• 10884450312459: D