| Primary Device ID | 06970953261107 |
| NIH Device Record Key | bfb1c1e0-71ff-4ed1-87d4-d4eaa313e912 |
| Commercial Distribution Discontinuation | 2020-12-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fitfaith |
| Version Model Number | M110 |
| Company DUNS | 544436982 |
| Company Name | Shenzhen Fitfaith Technology Co., Ltd |
| 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 | 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 | true |
| OTC Over-The-Counter | false |