| Primary Device ID | 07540191000357 |
| NIH Device Record Key | b9b61165-efcb-4c29-b0fb-fd6765721cb1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DC-EEG 3 DISC ELECTRODE KIT |
| Version Model Number | T8770 |
| Company DUNS | 209284132 |
| Company Name | Technologie de Pensée Ltée |
| 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 | true |
| Serial Number | false |
| 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 | 07540191000357 [Primary] |
| HCC | Device, Biofeedback |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-20 |
| Device Publish Date | 2017-08-31 |
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| 07540191000562 - NEUROINFINITI 2 | 2020-07-24 |