| Primary Device ID | 18054655016632 |
| NIH Device Record Key | 4c349c5c-2ecc-42c4-af4d-ac33da8359d1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Spes Medica Subdermal Needle Electrodes |
| Version Model Number | TT10MN4013D/10 |
| Company DUNS | 514029771 |
| Company Name | SPES MEDICA SRL |
| Device Count | 20 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |