TRIO CT® AS01135203MB

GUDID 50884908177621

13.5F X 20CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY

Medical Components, Inc.

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• Primary Device ID: 50884908177621
• NIH Device Record Key: 997cd4be-7ef4-4354-bb39-7cb7bd1cddcb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRIO CT®
• Version Model Number: AS01135203MB
• Catalog Number: AS01135203MB
• 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
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884908177626 [Primary]
GS1	50884908177621 [Package]; Contains: 00884908177626; Package: box [3 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: 2023-11-27
• Device Publish Date: 2023-11-17

On-Brand Devices [TRIO CT®]

• 50884908177645: 13.5F X 30CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY
• 50884908177638: 13.5F X 24CM TRIO-CT® TRIPLE LUMEN CATHTER MAX BARRIER PROCEDURE TRAY
• 50884908177621: 13.5F X 20CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY
• 50884908177614: 13.5F X 15CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY
• 50884908177607: 13.5F X 12CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY