Medtronic Diabetes Updater app iOS

GUDID 00763000532178

SFTWR MMT-6122 FOTA IOS V1.3.4

MEDTRONIC MINIMED, INC.

Patient health record information system application software

• Primary Device ID: 00763000532178
• NIH Device Record Key: 6babff9e-8e74-4cae-93c1-ead9980770bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Diabetes Updater app iOS
• Version Model Number: MMT-6122
• 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	00763000532178 [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.

• 00763000565039 - Medtronic Simplera™ Sensor: 2025-03-25 SENSOR MMT-5100JB SIMPLERA 1PK US
• 00763000565022 - Simplera™ Sensor: 2025-03-25 SENSOR MMT-5100JA SIMPLERA 5PK US
• 00763000565046 - Medtronic Simplera™ Sensor: 2025-03-25 KIT MMT-5101N SIMPLERA 5PK US
• 00763000829575 - Simplera™ Sensor: 2025-03-25 SENSOR MMT-5100JPA SIM 5PK PHARM US
• 00763000829650 - Simplera™ Sensor: 2025-03-25 KIT MMT-5101PN SIMPLERA 5PK PHARM US
• 00763000489953 - InPen Smart Insulin Delivery System: 2025-03-17 SOFTWARE MMT-8060 INSULIN PEN IOS APP
• 00763000489960 - InPen Smart Insulin Delivery System: 2025-03-17 SOFTWARE MMT-8061 INS PEN ANDROID APP
• 00763000984755 - CareLink™ Personal: 2025-01-10 PRODUCT SFTWR MMT-7333WW PERSONAL 15.0A