| Primary Device ID | 06970953260087 |
| NIH Device Record Key | ac17a999-bd23-43ce-86f8-a9d0f4d5f50b |
| Commercial Distribution Discontinuation | 2019-05-15 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fitfaith |
| Version Model Number | M230E |
| Company DUNS | 544436982 |
| Company Name | Shenzhen Fitfaith 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 | 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 |