| Primary Device ID | 05060229530356 |
| NIH Device Record Key | 15d9143b-53d5-4d27-a853-b641d0d12e63 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neurosign 100 Pre-Amplifier |
| Version Model Number | 1719-00 |
| 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 |
| Phone | +441994240798 |
| QA.RA@magstim.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060229530356 [Primary] |
| ETN | Stimulator, Nerve |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
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