DuraMax H787103028235

GUDID 00884450458433

Merit Medical Systems, Inc.

Double-lumen haemodialysis catheter, implantable

• Primary Device ID: 00884450458433
• NIH Device Record Key: d88d9ff1-63c0-4302-ac8f-65f9b3836526
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DuraMax
• Version Model Number: B
• Catalog Number: H787103028235
• 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: true
• 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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450458433 [Primary]

FDA Product Code

• MSD: Catheter, hemodialysis, implanted

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: 2026-03-30
• Device Publish Date: 2026-03-20

Devices Manufactured by Merit Medical Systems, Inc.

• 10884450029364 - Merit Medical®: 2026-04-01
• 10884450111731 - Merit Medical®: 2026-04-01
• 00884450220696 - Merit Medical®: 2026-04-01
• 10884450423629 - Merit Medical®: 2026-04-01
• 10884450425333 - Merit Medical®: 2026-04-01
• 20884450430815 - Merit Medical®: 2026-04-01
• 10884450430863 - Merit Medical®: 2026-04-01
• 00884450458426 - DuraMax®: 2026-04-01