| Primary Device ID | 00866387000411 |
| NIH Device Record Key | ad244116-2abd-425d-aeb4-68e2d4b23214 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | iTOVi |
| Version Model Number | ITS31 |
| Company DUNS | 095405024 |
| Company Name | ITOVI, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 |
| Phone | 877-483-3748 |
| Support@iTOVi.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00866387000411 [Primary] |
| GZO | Device, Galvanic Skin Response Measurement |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-09-12 |
| Device Publish Date | 2019-09-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ITOVI 87072963 5203312 Live/Registered |
ITOVI, LLC 2016-06-15 |
![]() ITOVI 87072939 5124258 Live/Registered |
ITOVI, LLC 2016-06-15 |
![]() ITOVI 87071375 5221340 Live/Registered |
ITOVI, LLC 2016-06-14 |
![]() ITOVI 77505840 not registered Dead/Abandoned |
Lee, Sang Eun 2008-06-23 |
![]() ITOVI 77505831 not registered Dead/Abandoned |
Lee, Sang Eun 2008-06-23 |