| Primary Device ID | 05415067024435 |
| NIH Device Record Key | fe434365-f468-419a-9f22-a5d60e7084a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroTherm |
| Version Model Number | RF-DGP-C |
| Catalog Number | RF-DGP-C |
| Company DUNS | 124023552 |
| Company Name | NEUROTHERM, 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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(855)478-5833 |
| customerservice@sjm.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05415067024435 [Primary] |
| IKD | CABLE, ELECTRODE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-05-08 |
| Device Publish Date | 2016-04-14 |
| 05415067021564 - Simplicity™ | 2018-11-08 Disposable Radiofrequency Electrode |
| 15415067021615 - NeuroTherm™ | 2018-11-08 Disposable Radiofrequency Electrode |
| 15415067022315 - NeuroTherm™ | 2018-11-08 Disposable Radiofrequency Electrode |
| 05415067026576 - NeuroTherm™ | 2018-11-08 PodiaTherm Disposable Kit |
| 05415067021243 - NeuroTherm™ | 2018-05-08 |
| 05415067021250 - NeuroTherm™ | 2018-05-08 |
| 05415067021298 - NeuroTherm™ | 2018-05-08 |
| 05415067021328 - NeuroTherm™ | 2018-05-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEUROTHERM 76063816 2575296 Live/Registered |
NEUROTHERM INC. 2000-06-06 |