Medtronic Diabetes Updater app Android

GUDID 00763000532161

SFTWR MMT-6121 FOTA ANDROID V1.3.4

MEDTRONIC MINIMED, INC.

Patient health record information system application software

• Primary Device ID: 00763000532161
• NIH Device Record Key: cc2a1452-af3d-4ad9-aa07-4f016f3d7e8d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Diabetes Updater app Android
• Version Model Number: MMT-6121
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000532161 [Primary]

FDA Product Code

• OUG: Medical device data system

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: 2023-05-23
• Device Publish Date: 2023-05-15

Devices Manufactured by MEDTRONIC MINIMED, INC.

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• 00763000984762 - CareLink™ Clinic: 2025-01-10 PRODUCT SOFTWARE MMT-7350 PROWEB 4.0A
• 00763000968168 - MiniMed™ Mobile: 2024-10-08 SFTWR MMT-6101 AHCL APP 2.7 ANDROID
• 00763000968175 - MiniMed™ Mobile: 2024-10-08 SFTWR MMT-6102 AHCL APP 2.7 IOS
• 00763000943257 - MiniMed™ Mobile: 2024-08-05 SFTWR MMT-6101 AHCL APP 2.6 ANDROID
• 00763000943264 - MiniMed™ Mobile: 2024-08-05 SFTWR MMT-6102 AHCL APP 2.6 IOS
• 00763000926106 - MiniMed™ 770G: 2024-07-09 PUMP MMT-1880L 770G US PRB
• 00763000926113 - MiniMed™ 770G: 2024-07-09 PUMP MMT-1880 770G US PRB