MEDTRONIC CARELINK® MONITOR

GUDID 00643169690943

MON 2490C17 CARELINK C17 VISIA CRTD USA

MEDTRONIC, INC.

Cardiac pulse generator reader, home-use Cardiac pulse generator reader, home-use

• Primary Device ID: 00643169690943
• NIH Device Record Key: f57dfdc5-41a3-4fa4-bcb2-82766cff62a3
• Commercial Distribution Discontinuation: 2018-06-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MEDTRONIC CARELINK® MONITOR
• Version Model Number: 2490C17
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• 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

Operating and Storage Conditions

• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169690943 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P890003

FDA Product Code

• OSR: Pacemaker/icd/crt non-implanted components

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-02-18

On-Brand Devices [MEDTRONIC CARELINK® MONITOR]

• 00643169690943: MON 2490C17 CARELINK C17 VISIA CRTD USA
• 00643169376823: MON 2490C16 USA C16 HPMRI
• 00643169341050: MON 2490C15 CL 60601 3 ED HCM USA RFB
• 00643169334717: MON 2490C15 CL 60601 3 ED LCM USA RFB
• 00643169191815: MON 2490C15 USA C15 60601