| Primary Device ID | 00860001532777 |
| NIH Device Record Key | f01ff537-4f89-4cc2-bd4e-bb25b496bda9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | True Integral |
| Version Model Number | DMT-4320 |
| Company DUNS | 117033737 |
| Company Name | TRUE INTEGRAL INC |
| 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 | true |
| 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 | 00860001532777 [Primary] |
| FLL | Thermometer, Electronic, Clinical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-20 |
| Device Publish Date | 2019-05-10 |
| 00860001532760 | Upper Arm Blood Pressure Monitor |
| 00860001532753 | Digital thermometer |
| 00860001532746 | Dual mode thermometer |
| 00860001532739 | B02 |
| 00860001532708 | B05 |
| 00860001532777 | Digital thermometer |
| 00860003079706 | Intelligent Mesh Nebulizer |
| 00860003079737 | UPER ARM BLOOD PRESSURE MONITOR |
| 00860003079713 | INFRARED FOREHEAD THERMOMETER |
| 00860003079744 | UPER ARM BLOOD PRESSURE MONITOR |
| 00860003079720 | No- contact infarared body thermometer |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRUE INTEGRAL 88614238 not registered Live/Pending |
True Integral Inc. 2019-09-12 |