| Primary Device ID | 00613994951151 |
| NIH Device Record Key | 0fcb59d8-f3fe-40ec-b66c-d03c1888014b |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 3708160 |
| Company DUNS | 796986144 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Lot Batch | false |
| Serial Number | true |
| 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Length | 60 Centimeter |
| Length | 60 Centimeter |
| Length | 60 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994951151 [Primary] |
| LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
| 00199150016716 - NA | 2025-06-02 CUSTOM PACK BB8H19R2 ASSIST |
| 20199150019605 - NA | 2025-06-02 CUSTOM PACK BB9E36R2 5PK PACK 3 |
| 00199150019854 - NA | 2025-06-02 CUSTOM PACK BB11M65R2 ADULT ECC 1/4 |
| 00199150019861 - NA | 2025-06-02 CUSTOM PACK BB12B99R7 1/4 CENTRI PK |
| 20199150019889 - NA | 2025-06-02 CUSTOM PACK BB11Q69R1 10PK ANH PACK |
| 00199150019892 - NA | 2025-06-02 CUSTOM PACK BB8S58R4 3/8 SUPP |
| 00199150019908 - NA | 2025-06-02 CUSTOM PACK BB8T55R4 1/4 SUPP |
| 00199150019915 - NA | 2025-06-02 CUSTOM PACK BB5227R13 ASSIST |