MiniMed™ Mobile

GUDID 00763000968168

SFTWR MMT-6101 AHCL APP 2.7 ANDROID

MEDTRONIC MINIMED, INC.

Self-care monitoring/reporting software

• Primary Device ID: 00763000968168
• NIH Device Record Key: b0680b48-c6c2-446d-b033-377ac3d3464a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MiniMed™ Mobile
• Version Model Number: MMT-6101
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000968168 [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: 2024-10-08
• Device Publish Date: 2024-09-30

On-Brand Devices [MiniMed™ Mobile]

• 00763000480677: SFTWR MMT-6104 MM MBL CLIN IOS 1.0.0
• 00763000480660: SFTWR MMT-6103 MM MBL CLIN ANDRD 1.0.0
• 00763000416676: SFTWR MMT-6102 AHCL 1.3 APP IOS
• 00763000827793: SFTWR MMT-6102 AHCL 2.1.0 APP IOS
• 00763000827786: SFTWR MMT-6101 AHCL 2.1.0 APP ANDROID
• 00763000521301: SFTWR MMT-6104 MM MBL CLIN IOS 2.0.2
• 00763000867638: SFTWR MMT-6102 AHCL APP 2.2 IOS
• 00763000910150: SFTWR MMT-6102 AHCL APP 2.5 IOS
• 00763000943264: SFTWR MMT-6102 AHCL APP 2.6 IOS
• 00763000943257: SFTWR MMT-6101 AHCL APP 2.6 ANDROID
• 00763000968175: SFTWR MMT-6102 AHCL APP 2.7 IOS
• 00763000968168: SFTWR MMT-6101 AHCL APP 2.7 ANDROID