TRIPLE LUMEN INFUSION CATHETERSTRIPLE LUMEN INFUSION CATHETERS

GUDID 50884908097004

7F X 20CM TRIPLE LUMEN7F X 20CM INFUSION CATHETER TRAYINFUSION C

Medical Components, Inc.

Central venous catheter

• Primary Device ID: 50884908097004
• NIH Device Record Key: d093fc8f-8d47-46e4-8e93-dd71f05e1034
• Commercial Distribution Discontinuation: 2018-01-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TRIPLE LUMEN INFUSION CATHETERSTRIPLE LUMEN INFUSION CATHETERS
• Version Model Number: MC3L-8S-PA
• 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	00884908097009 [Primary]
GS1	50884908097004 [Package]; Contains: 00884908097009; Package: box [10 Units]; Discontinued: 2018-01-11; Not in Commercial Distribution

FDA Product Code

• JCY: CATHETER, INFUSION

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-15
• Device Publish Date: 2017-03-16

Devices Manufactured by Medical Components, Inc.

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• 50884908187620 - SLX Hemo-Cath®: 2026-03-30 14F X 24CM SLX MAX BARRIER TRAY
• 50884908187637 - SLX HEMO-CATH®: 2026-03-30 14F X 30CM SLX MAX BARRIER TRAY
• 30884908188456 - MICRO-STICK SET: 2026-02-27 4F (1.0MM ID) X 9CM STIFF MICRO-STICK® INTRODUCER SET WITH NITINOL GUIDEWIRE WITH RADIOPAQUE TIP
• 30884908188463 - MICRO-STICK SET: 2026-02-27 4F (1.0MM ID) X 9CM REGULAR MICRO-STICK® INTRODUCER SET WITH NITINOL GUIDEWIRE WITH RADIOPAQUE TIP
• 50884908188474 - MICRO-STICK SET: 2026-02-27 5F (1.0MM ID) X 9CM STIFF MICRO-STICK® INTRODUCER SET WITH NITINOL GUIDEWIRE WITH RADIOPAQUE TIP
• 50884908188481 - MICRO-STICK SET: 2026-02-27 5F (1.0MM ID) X 9CM REGULAR MICRO-STICK® INTRODUCER SET WITH NITINOL GUIDEWIRE WITH RADIOPAQUE TIP