EOPA CAP™

GUDID 20613994888642

CANNULA 77922 EOPA CAP NONVENT 22FR

MEDTRONIC, INC.

Cardiopulmonary bypass cannula, arterial

• Primary Device ID: 20613994888642
• NIH Device Record Key: 5acb10fc-aeba-4658-9335-58b66e1e58e8
• Commercial Distribution Discontinuation: 2017-08-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: EOPA CAP™
• Version Model Number: 77922
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• 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
• 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
• 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 Dimensions

• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994888648 [Unit of Use]
GS1	20613994888642 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031518

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: 2016-09-09

On-Brand Devices [EOPA CAP™]

• 20643169486236: CANNULA 77822 EOPA CAP 22FR 10PK 10L
• 20643169486229: CANNULA 77820 EOPA CAP 20FR 10PK 10L
• 20643169486212: CANNULA 77818 EOPA CAP 18FR 10PK 10L
• 20613994888642: CANNULA 77922 EOPA CAP NONVENT 22FR
• 20613994888635: CANNULA 77920 EOPA CAP NONVENT 20FR
• 20613994888628: CANNULA 77918 EOPA CAP NONVENT 18FR