CareLink™ Connect

GUDID 00763000791391

SFTWR MMT-6111 CP ANDROID V3.2.1 OUS

MEDTRONIC MINIMED, INC.

Patient health record information system application software

• Primary Device ID: 00763000791391
• NIH Device Record Key: de730394-42a0-4f17-be33-efd79582fea4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CareLink™ Connect
• Version Model Number: MMT-6111
• Company DUNS: 849626338
• Company Name: MEDTRONIC MINIMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000791391 [Primary]

FDA Product Code

• PKU: Insulin pump secondary display

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-29
• Device Publish Date: 2024-03-21

On-Brand Devices [CareLink™ Connect]

• 00763000480653: SFTWR MMT-6114 CL CONN CLIN IOS 2.1.1
• 00763000480646: SFTWR MMT-6113 CL CONN CLIN ANDRD 2.1.1
• 00763000437794: SFTWR MMT-6111 CP ANDROID V2.3.0 US
• 00763000437787: SFTWR MMT-6112 CP IOS V2.3.0 US
• 00763000432652: SFTWR MMT-6111 CP ANDROID V2.2.0 OUS
• 00763000827304: SFTWR MMT-6112 CP IOS V3.1.0 US
• 00763000827298: SFTWR MMT-6111 CP ANDROID V3.1.0 US
• 00763000791391: SFTWR MMT-6111 CP ANDROID V3.2.1 OUS