| Primary Device ID | 00885074200330 |
| NIH Device Record Key | c59f51e9-b06c-4bd9-a826-77294759dcd8 |
| Commercial Distribution Discontinuation | 2018-08-13 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 355032 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885074200330 [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 | 4 |
| Public Version Date | 2018-10-02 |
| Device Publish Date | 2014-09-23 |
| 00199150003624 - NA | 2025-04-11 CUSTOM PACK BB5723R37 CHR LINF |
| 00199150003631 - NA | 2025-04-11 CUSTOM PACK BB11Y69R2 SATELLITE |
| 00199150003969 - NA | 2025-04-11 CUSTOM PACK BB10Z37R8 PEDS PACK |
| 00199150003976 - NA | 2025-04-11 CUSTOM PACK BB11R40R1 TRANS PORT |
| 00199150004041 - NA | 2025-04-11 CUSTOM PACK BB8D33R18 PUMP PK |
| 20199150004069 - NA | 2025-04-11 CUSTOM PACK BB7U92R3 5PK BRIDGE PK |
| 20199150004083 - NA | 2025-04-11 CUSTOM PACK BB10V11R1 5PK EXTENSION LIN |
| 20199150004120 - NA | 2025-04-11 CUSTOM PACK BB9R13R13 4PK PLEG PACK |