MC2X®

GUDID 20643169463022

CANNULA 91429 MC2X 29/29/29FR 10PK 17L

MEDTRONIC, INC.

Cardiopulmonary bypass cannula, venous

• Primary Device ID: 20643169463022
• NIH Device Record Key: 6ffb2aa9-8008-48a0-80f6-759a81f58ff0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MC2X®
• Version Model Number: 91429
• 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: 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: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French
• Catheter Gauge: 29 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169463028 [Primary]
GS1	20643169463022 [Package]; Contains: 00643169463028; Package: PK [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140165

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: 2016-06-16

On-Brand Devices [MC2X®]

• 00643169560512: CANN CB91429C MC2X VEN 29/29/29FR 17L
• 00643169560505: CANN CB91429 MC2X 29/29/29FR 17L
• 20643169490158: CANNULA 91429C MC2X VEN 29FR 10PK 17L
• 20643169463022: CANNULA 91429 MC2X 29/29/29FR 10PK 17L
• 00643169159280: CANN CB91437C MC2X 29/46/37F17
• 00643169159273: CANN CB91437 MC2X 29/46/37F 17
• 00643169159266: CANN CB91429C MC2X VEN 29/29/29F
• 00643169159259: CANN CB91429 MC2X VEN 29/29/29FR
• 20613994887058: CANNULA 91437 MC2X 29/37FR 10PK 17L
• 20613994887041: CANNULA 91437C MC2X 29/37FR CON 10P 17L