GUDID 20721902838433

CANNULA KIT DLP3E16R 5PK SPTRKS C

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set

• Primary Device ID: 20721902838433
• NIH Device Record Key: 266ed435-2424-40e9-91e2-0befd286af37
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DLP3E16R
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 5
• 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	00721902838439 [Unit of Use]
GS1	20721902838433 [Primary]

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: 2016-06-05

Devices Manufactured by MEDTRONIC, INC.

• 00763000449711 - INTERSTIM® II: 2025-12-16 INS 3058 IS II EMAN US
• 00199150062980 - NA: 2025-12-15 CUSTOM PACK BB9H69R15 HLO H/LW/VAV
• 00199150063390 - NA: 2025-12-15 CUSTOM PACK 10D80R1 ACC TEMP PROBE
• 00199150063550 - NA: 2025-12-15 CUSTOM PACK BB7W91R29 HLO OH PACK2
• 00763000929374 - NA: 2025-12-15 WIRELESS RECHARGER P720R1 ALTAVIVA
• 20199150061970 - NA: 2025-12-08 CUSTOM PACK BB12R02R3 5PK ACC STRNG SUC
• 00199150062027 - NA: 2025-12-08 CUSTOM PACK BB12R85R AVL 3/8 ECCPK
• 20199150062229 - NA: 2025-12-08 CUSTOM PACK BB1Q47R3 5PK ACC TABLE