| Primary Device ID | 00643169273030 |
| NIH Device Record Key | d0fc0f92-41fc-4df4-8557-6e225cde2b00 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 3708360 |
| 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 |
| Length | 60 Centimeter |
| Length | 60 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169273030 [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 |
| 20763000950280 - NA | 2024-05-07 CUSTOM PACK BB10N53R3 5PK ACCESSORY |
| 00763000950699 - NA | 2024-05-07 CUSTOM PACK 5D56R9 NEURO FLOWS |
| 00763000841591 - Cardioblate™ Gemini™-s | 2024-05-06 CARDIOBLATE GEMINI-S 49260 EN |
| 00763000949341 - NA | 2024-05-06 CUSTOM PACK BB12A73R5 AV LOOP |
| 20763000949369 - NA | 2024-05-06 CUSTOM PACK BB12F71R2 4PK LOYOLA CPG |
| 00763000949372 - NA | 2024-05-06 CUSTOM PACK BB11L23R8 UTMC SUPP PK |
| 20763000950105 - NA | 2024-05-06 CUSTOM PACK BB12G65R 5PK TAPER |
| 00763000950118 - NA | 2024-05-06 CUSTOM PACK CB3Z71R24 PRIMARY |