| Primary Device ID | 06978181510257 |
| NIH Device Record Key | d3a8e8d3-a7d8-41f1-b2a4-058e22ed1d57 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QOLIGHT |
| Version Model Number | Remyfx-D3F |
| Company DUNS | 714815435 |
| Company Name | Wuhan Qolight Technology Co., Ltd. |
| 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 | true |
| 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 |