| Primary Device ID | 00613994756596 |
| NIH Device Record Key | 3a84a203-82c0-4603-bb39-7c78faba791c |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 3875-60 |
| 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 | 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Length | 60 Centimeter |
| Length | 60 Centimeter |
| Length | 60 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994756596 [Primary] |
| GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (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 | 2015-06-08 |
| 00199150006434 - NA | 2025-04-22 CUSTOM PACK BB11P23R4 LARGO DUAL V |
| 00199150006465 - NA | 2025-04-22 CUSTOM PACK BB12E01R8 MAINPCK |
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| 20199150006896 - NA | 2025-04-22 CUSTOM PACK BB10Y97R1 5PK MANIFOLD |
| 20199150006919 - NA | 2025-04-22 CUSTOM PACK BB10Y99R1 10PK ARTERIAL Y |
| 00199150006922 - NA | 2025-04-22 CUSTOM PACK BB11Q27R2 MANIFOLD |