12F TRI-FLOW TRIPLE LUMEN CATHETER AC0212201

GUDID 50884908182854

12F X 20CM TRI-FLOW TRIPLE LUMEN CATHETER SET W/CURVED EXTENSIONS

Medical Components, Inc.

Triple-lumen haemodialysis catheter

• Primary Device ID: 50884908182854
• NIH Device Record Key: fbab65c4-2f35-4be3-9504-c65b2ff212eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 12F TRI-FLOW TRIPLE LUMEN CATHETER
• Version Model Number: AC0212201
• Catalog Number: AC0212201
• Company DUNS: 038000253
• Company Name: Medical Components, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884908182859 [Primary]
GS1	50884908182854 [Package]; Contains: 00884908182859; Package: box [5 Units]; In Commercial Distribution

FDA Product Code

• NIE: Catheter, hemodialysis, triple lumen, non-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: 2025-03-26
• Device Publish Date: 2025-03-18

On-Brand Devices [12F TRI-FLOW TRIPLE LUMEN CATHETER]

• 50884908182885: 12F X 24CM TRI-FLOW TRIPLE LUMEN CATHETER SET
• 50884908182878: 12F X 20CM TRI-FLOW TRIPLE LUMEN CATHETER SET
• 50884908182861: 12F X 15CM TRI-FLOW TRIPLE LUMEN CATHETER SET
• 50884908182854: 12F X 20CM TRI-FLOW TRIPLE LUMEN CATHETER SET W/CURVED EXTENSIONS
• 50884908182847: 12F X 15CM TRI-FLOW TRIPLE LUMEN CATHETER SET W/CURVED EXTENSIONS