| Primary Device ID | 00763000875688 |
| NIH Device Record Key | d3912d60-b635-443c-b274-8b94c35bbb61 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Synergy EZ™ |
| Version Model Number | 7435-RFB |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000875688 [Primary] |
| LGW | Stimulator, spinal-cord, totally implanted for pain relief |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-24 |
| Device Publish Date | 2023-11-16 |
| 00763000449711 - INTERSTIM® II | 2025-12-16 INS 3058 IS II EMAN US |
| 00199150062980 - NA | 2025-12-15 CUSTOM PACK BB9H69R15 HLO H/LW/VAV |
| 00199150063390 - NA | 2025-12-15 CUSTOM PACK 10D80R1 ACC TEMP PROBE |
| 00199150063550 - NA | 2025-12-15 CUSTOM PACK BB7W91R29 HLO OH PACK2 |
| 00763000929374 - NA | 2025-12-15 WIRELESS RECHARGER P720R1 ALTAVIVA |
| 20199150061970 - NA | 2025-12-08 CUSTOM PACK BB12R02R3 5PK ACC STRNG SUC |
| 00199150062027 - NA | 2025-12-08 CUSTOM PACK BB12R85R AVL 3/8 ECCPK |
| 20199150062229 - NA | 2025-12-08 CUSTOM PACK BB1Q47R3 5PK ACC TABLE |