Mi¯RCSP™

GUDID 20643169086962

CANNULA 94113TD MIRCSP 13F MAN 2P 17

MEDTRONIC, INC.

Coronary sinus cannula

• Primary Device ID: 20643169086962
• NIH Device Record Key: 8747d146-89c3-43eb-be9e-be6672e62a55
• Commercial Distribution Discontinuation: 2018-10-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Mi¯RCSP™
• Version Model Number: 94113TD
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 2
• 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

Device Dimensions

• Catheter Gauge: 13 French
• Catheter Gauge: 13 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169086968 [Unit of Use]
GS1	20643169086962 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090869

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: 4
• Public Version Date: 2018-12-11
• Device Publish Date: 2016-06-02

On-Brand Devices [Mi¯RCSP™]

• 20643169086962: CANNULA 94113TD MIRCSP 13F MAN 2P 17
• 20643169086221: CANNULA 94113TDT MiRCSP 13 MAN OUS 2P 17
• 20643169086214: CANNULA 94533TD MiRCSP 13 AUTO WW 2P 17
• 20643169086207: CANNULA 94533TDT MiRCSP 13 AUTO WW 2P17