| Primary Device ID | 06430056480428 |
| NIH Device Record Key | 2ce5de85-7e60-46fc-a2ad-37ad5890b6e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Finger response pad |
| Version Model Number | NM20928X |
| Company DUNS | 538025107 |
| Company Name | Megin Oy |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06430056480428 [Primary] |
| OLY | Magnetoencephalograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-04-21 |
| Device Publish Date | 2025-04-11 |
| 06430056480039 - MaxFilter™ 2.2 | 2025-06-02 MaxFilter™ is used with Elekta Neuromag®, Elekta Neuromag® TRIUX and TRIUXTM neo in suppressing magnetic interference and in |
| 06430056480404 - MEGreview™ | 2025-06-02 MEGreview™ is used for detection and localization of epileptic spontaneous brain activity. In addition, MEGreview™ may be us |
| 06430056480411 - TRIUX™ neo | 2025-06-02 TRIUX™ neo non-invasively measures the magnetoencephalographic (MEG) signals (and, optionally, electro-encephalographic (EEG) |
| 06430056480428 - Finger response pad | 2025-04-21A finger response pad for detecting patient responses. |
| 06430056480428 - Finger response pad | 2025-04-21 A finger response pad for detecting patient responses. |