| Primary Device ID | 06970663420085 |
| NIH Device Record Key | 9b023537-0f1a-4910-bb2e-536d46c3e8d4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UTK |
| Version Model Number | H-12G1-L |
| Company DUNS | 544434373 |
| Company Name | UTK TECHNOLOGY(SHENZHEN)LIMITED |
| 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 | 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 | true |