| Primary Device ID | 00850005944911 |
| NIH Device Record Key | 1a01c4f7-55f2-4ebf-b749-8635ecd76d07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroStar Headrest |
| Version Model Number | 81-72026-00U |
| Company DUNS | 134960348 |
| Company Name | NEURONETICS, 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 | 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 | 877-600-7555 |
| customersupport@neurostar.com | |
| Phone | 877-600-7555 |
| customersupport@neurostar.com | |
| Phone | 877-600-7555 |
| customersupport@neurostar.com | |
| Phone | 877-600-7555 |
| customersupport@neurostar.com | |
| Phone | 877-600-7555 |
| customersupport@neurostar.com | |
| Phone | 877-600-7555 |
| customersupport@neurostar.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850005944911 [Primary] |
| QCI | Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-17 |
| Device Publish Date | 2025-12-09 |
| 00850005944348 | The NeuroStar Headrest can be adjusted to the patient's comfort. |
| 00850005944911 | The NeuroStar Headrest can be adjusted to the patient's comfort. NeuroStar Headrest Assembly Dom |