| Primary Device ID | 00885074200194 |
| NIH Device Record Key | df1effd7-90ba-4867-a0f1-931e660a30a7 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 355026 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885074200194 [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 |
| 00763000960308 - NA | 2024-07-09 CUSTOM PACK BB12C30R7 NPR IMC |
| 00763000960407 - NA | 2024-07-09 CUSTOM PACK BB12G16R3 UCHICAGO CPB |
| 00763000228699 - NA | 2024-07-08 KIT 20MRK ARCTIC FRNT MANETRACT GLB TIJ |
| 00763000957193 - NA | 2024-07-08 CUSTOM PACK BB7M46R25 SCV ADLT |
| 20763000960272 - NA | 2024-07-08 CUSTOM PACK 10R91R5 10PK LRTXBYPS |
| 20763000960296 - NA | 2024-07-08 CUSTOM PACK SSBB12D06R4 4PK RESOXY BYPA |
| 00763000879273 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US EMANUAL |
| 00763000879280 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US REFURB EMAN |