| Primary Device ID | G180DIOWAVE250WLS0 |
| NIH Device Record Key | ac6f5c35-e132-4576-963d-5defa1aa2ee8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DIOWAVE |
| Version Model Number | 250WLS |
| Company DUNS | 725228743 |
| Company Name | Wuhan PHOMED 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 | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |