CentrosFLO® CENFT31K

GUDID 10884450295608

Merit Medical Systems, Inc.

Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable

• Primary Device ID: 10884450295608
• NIH Device Record Key: ca4533c0-36df-4722-bbae-db7b0786d929
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CentrosFLO®
• Version Model Number: A
• Catalog Number: CENFT31K
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450295601 [Primary]
GS1	10884450295608 [Package]; Contains: 00884450295601; Package: [5 Units]; In Commercial Distribution

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: 2024-03-20
• Device Publish Date: 2024-03-12

On-Brand Devices [CentrosFLO®]

• 10884450295585: 00884450295588
• 10884450295547: 00884450295540
• 10884450276126: 00884450276129
• 10884450276089: 00884450276082
• 20884450276055: 00884450276051
• 10884450200060: 00884450200063
• 10884450200053: 00884450200056
• 10884450200022: 00884450200025
• 10884450200015: 00884450200018
• 10884450200008: 00884450200001
• 10884450199999: 00884450199992
• 20884450199972: 00884450199978
• 20884450199958: 00884450199954
• 20884450199910: 00884450199916
• 20884450199903: 00884450199909
• 20884450199880: 00884450199886
• 10884450190439: 00884450190432
• 10884450276065: 00884450276068
• 10884450725914: 00884450725917
• 10884450295578: 00884450295571
• 10884450295561: 00884450295564
• 10884450295554: 00884450295557
• 10884450726010: 00884450726013
• 10884450276102: 00884450276105
• 10884450276096: 00884450276099
• 10884450726003: 00884450726006
• 10884450725990: 00884450725993
• 10884450276140: Initial Release
• 10884450295530: A
• 10884450295608: A