GUDID 20613994911524

CANNULA KIT DLP6X23R 5PK UNIV HSP

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set

• Primary Device ID: 20613994911524
• NIH Device Record Key: c2e459f8-e31a-41e1-af65-725041289c57
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DLP6X23R
• 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	00613994911520 [Primary]
GS1	20613994911524 [Package]; Contains: 00613994911520; 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: 2016-05-21

Devices Manufactured by MEDTRONIC, INC.

• 20763000980096 - NA: 2025-08-25 IMPEDANCE PATCH AFR-00015
• 20763000980119 - NA: 2025-08-25 MAGNETIC PATCH AFR-00021
• 00199150039371 - NA: 2025-08-22 CUSTOM PACK BB11U72R1 P/T
• 00199150040872 - NA: 2025-08-22 CUSTOM PACK BB4K95R22 HLO PERFNPLEG
• 00199150041145 - NA: 2025-08-22 CUSTOM PACK BB12Q87R1 HLN VAMC NASH
• 00199150041978 - NA: 2025-08-22 CUSTOM PACK BB10F40R2 ACCESORY
• 00199150041299 - NA: 2025-08-19 CUSTOM PACK BB8E60R12 EVL PED E
• 20199150041118 - NA: 2025-08-18 CUSTOM PACK BB12E30R1 10PK ACC BRIDGE