SenStar Treatment Link
GUDID 10850005944222
NEURONETICS, INC.
Magnetic neural stimulation system| Primary Device ID | 10850005944222 |
| NIH Device Record Key | cedde0c8-ca8b-4a44-bf70-5bb0e5f64aa2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SenStar Treatment Link |
| Version Model Number | 81-70000-000 |
| 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 | true |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850005944225 [Primary] |
| GS1 | 10850005944222 [Package] Contains: 00850005944225 Package: Inner Pack [5 Units] In Commercial Distribution |
| GS1 | 20850005944229 [Package] Package: Inner Pack [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- deNovo: DEN070003
FDA Product Code
| OBP | Transcranial Magnetic Stimulator |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-13 |
| Device Publish Date | 2022-10-05 |
On-Brand Devices [SenStar Treatment Link]
| 10850005944222 | 81-70000-000 |
| 10850005944635 | 81-70100-000 |
Trademark Results [SenStar Treatment Link]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SENSTAR TREATMENT LINK 77172671 3377575 Dead/Cancelled |
Neuronetics, Inc. 2007-05-04 |
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