| Primary Device ID | 05060229532602 |
| NIH Device Record Key | 7a2f33da-ea87-4eed-bfb2-dee2d54abf21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Horizon 3.0 Interface Unit (Nav) |
| Version Model Number | 5445-00 |
| Company DUNS | 500375274 |
| Company Name | THE MAGSTIM COMPANY LIMITED |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060229532602 [Primary] |
| OBP | Transcranial Magnetic Stimulator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-12-29 |
| Device Publish Date | 2021-12-21 |
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