PRO-LINE® CT PRESSURE INJECTABLE CVC (ISOPLAST) MD28036301

GUDID 50884908140601

6F X 60CM TRIPLE LUMEN PRO-LINE® CT BASIC IR SET

Medical Components, Inc.

Centrally-inserted central venous catheter

• Primary Device ID: 50884908140601
• NIH Device Record Key: 89be6014-f931-4a0a-b88d-87e166979495
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-LINE® CT PRESSURE INJECTABLE CVC (ISOPLAST)
• Version Model Number: MD28036301
• Catalog Number: MD28036301
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884908140606 [Primary]
GS1	50884908140601 [Package]; Contains: 00884908140606; 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: 2023-05-31
• Device Publish Date: 2023-05-23

On-Brand Devices [PRO-LINE® CT PRESSURE INJECTABLE CVC (ISOPLAST)]

• 50884908172992: 5F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908172985: 6F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908172961: 5F X 55CM DUAL LUMEN PRO-LINE® CT W/CUFF @ 5CM BASIC IR SET
• 50884908155988: 6F X 60CM DUAL LUMEN PRO-LINE® CT W/CUFF @ 5CM BASIC IR SET
• 50884908140618: 7F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908140601: 6F X 60CM TRIPLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908140465: 7F X 60CM DUAL LUMEN PRO-LINE® CT BASIC IR SET
• 50884908180515: 6F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908180645: 7F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET
• 50884908180539: 6F X 60CM DUAL LUMEN PRO-LINE® CT W/CUFF @ 5CM BASIC IR SET
• 50884908180492: 5F X 55CM DUAL LUMEN PRO-LINE® CT W/CUFF @ 5CM BASIC IR SET
• 50884908180478: 5F X 60CM SINGLE LUMEN PRO-LINE® CT BASIC IR SET