| Primary Device ID | 00643169164413 |
| NIH Device Record Key | 52b20b84-0ccd-474a-bf75-0d76bce9957b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sen-Serter© |
| Version Model Number | MMT-7500 |
| Company DUNS | 849626338 |
| Company Name | MEDTRONIC MINIMED, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169164413 [Primary] |
| MDS | Sensor, glucose, invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-10-01 |
| 00763000926106 - MiniMed™ 770G | 2024-07-09 PUMP MMT-1880L 770G US PRB |
| 00763000926113 - MiniMed™ 770G | 2024-07-09 PUMP MMT-1880 770G US PRB |
| 00763000924089 - MiniMed™ 780G | 2024-06-17 PUMP MMT-1884 780G US MG A2.01 6.21U |
| 00763000924096 - MiniMed™ 780G | 2024-06-17 PUMP MMT-1884 780G US A2.01 6.21U PRB |
| 00763000924102 - MiniMed™ 780G | 2024-06-17 KIT MMT-1894 780G US MG A2.01 6.21U |
| 00763000924119 - MiniMed™ 780G | 2024-06-17 KIT MMT-1894MD 780G US A2.01 6.21U |
| 00763000827182 - inpen™ | 2024-06-11 KIT MMT-105NNBLNA INPEN NOVONORDISK BLUE |
| 00763000827199 - inpen™ | 2024-06-11 KIT MMT-105NNGYNA INPEN NOVONORDISK GREY |