GUDID 20613994667773

CANNULA KIT DLP2X93R3 5PK SPARTANB

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set

• Primary Device ID: 20613994667773
• NIH Device Record Key: ad111001-b706-4ab0-a8ce-0c163bb9986d
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DLP2X93R3
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994667779 [Primary]
GS1	20613994667773 [Package]; Contains: 00613994667779; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K924529

FDA Product Code

• DWF: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-05-22

Devices Manufactured by MEDTRONIC, INC.

• 20763000394091 - DxTerity™: 2025-01-28 DXT6JL45X DXT 6F 5PK 125CM JL45
• 20763000395180 - DxTerity™ TRA: 2025-01-28 CATH U5ULTRA35 DXT 5F 5PK 100CM UL35
• 00763000993924 - NA: 2025-01-28 CUSTOM PACK BB10Y59R12 FUSION
• 00763000993931 - NA: 2025-01-28 CUSTOM PACK BB7M46R26 SCV ADLT
• 00763000993948 - NA: 2025-01-28 CUSTOM PACK BB11U59R5 BYPASS TUBING
• 00763000993955 - NA: 2025-01-28 CUSTOM PACK BB8M65R3 RIDEOUT
• 08033477072012 - Pacific™ Plus: 2025-01-28 CATH PCP060300090 PLUS US D6L300UL900
• 08033477072029 - Pacific™ Plus: 2025-01-28 CATH PCP060300150 PLUS US D6L300UL1500