Pro-Line® CT MRCTC72001

GUDID 50884908180614

7F X 60CM DUAL Pro-Line® CT BASIC SET

Medical Components, Inc.

Centrally-inserted central venous catheter

• Primary Device ID: 50884908180614
• NIH Device Record Key: 9cb47960-970a-4de0-8add-7250d16c42c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pro-Line® CT
• Version Model Number: MRCTC72001
• Catalog Number: MRCTC72001
• Company DUNS: 038000253
• Company Name: Medical Components, 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: 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	00884908180619 [Primary]
GS1	50884908180614 [Package]; Contains: 00884908180619; Package: box [5 Units]; In Commercial Distribution

FDA Product Code

• LJS: Catheter, intravascular, therapeutic, long-term greater than 30 days

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: 2024-09-23
• Device Publish Date: 2024-09-13

On-Brand Devices [Pro-Line® CT]

• 50884908107475: 5F X 55CM DUAL LUMEN Pro-Line® CT W/CUFF @ 2CM BASIC IR SET
• 50884908107468: 5F X 55CM DUAL LUMEN Pro-Line® CT W/CUFF @ 5CM BASIC IR SET
• 50884908105051: 6F X 60CM TRIPLE Pro-Line® CT OR SET W/0.038" WIRE
• 50884908104931: 7F X 60CM DUAL PRO-LINE® CT OR SET W/ .038 WIRE
• 50884908104870: 7F X 60CM SINGLE PRO-LINE® CT OR SET W/ .038" WIRE
• 50884908104863: 6F X 60CM DUAL Pro-Line® CT OR SET W/ .038" WIRE
• 30884908104852: 6F X 60CM SINGLE PRO-LINE® CT OR SET W/ .038" WIRE
• 50884908097752: 6F X 60CM TRIPLE LUMEN Pro-Line® CT BASIC IR SET
• 50884908097172: 7F X 60CM DUAL Pro-Line® CT BASIC IR SET
• 50884908097165: 7F X 60CM SINGLE Pro-Line® CT BASIC IR SET
• 30884908094283: 6F X 60CM SINGLE LUMEN Pro-Line® CT W/ CUFF @ 2CM BASIC IR SET
• 30884908094276: 6F X 60CM DUAL LUMEN Pro-Line® CT W/ CUFF @ 2CM BASIC IR SET
• 50884908094263: 5F X 60CM SINGLE LUMEN Pro-Line® CT w/ CUFF @2CM BASIC IR SET
• 50884908039226: 6F X 60CM DUAL PRO-LINE® CT BASIC IR SET
• 50884908034641: 7F X 60CM DUAL LUMEN PRO-LINE® CT BASIC IR SET
• 50884908034634: 7F X 60CM SINGLE LUMEN Pro-Line® CT BASIC IR SET
• 30884908034623: 6F X 60CM DUAL LUMEN Pro-Line® CT W/CUFF @ 5CM BASIC IR SET
• 50884908034610: 6F X 60CM SINGLE LUMEN Pro-Line® CT BASIC IR SET
• 50884908034603: 5F X 60CM SINGLE LUMEN Pro-Line® CT BASIC IR SET
• 50884908180614: 7F X 60CM DUAL Pro-Line® CT BASIC SET
• 50884908180607: 7F X 60CM SINGLE Pro-Line® CT BASIC SET