| Primary Device ID | 00869378000117 |
| NIH Device Record Key | 183659fb-a633-4aea-99a9-4817a9a7811b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroStar TMS Therapy System |
| Version Model Number | NeuroStar 3.0 US |
| Catalog Number | 81-02315-000 |
| Company DUNS | 134960348 |
| Company Name | NEURONETICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00869378000117 [Primary] |
| OBP | Transcranial Magnetic Stimulator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-20 |
| 00869378000155 | Upgrade Kit 3.0 US |
| 00869378000148 | Multi-Coil Option Upgrade |
| 00869378000117 | NeuroStar 3.0 US |
| 00869378000100 | . |