| Primary Device ID | 00853023006180 |
| NIH Device Record Key | 2148aa6f-d49a-4587-a278-dd9df7953c56 |
| Commercial Distribution Discontinuation | 2018-04-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Cerner Motion Health |
| Version Model Number | MotionHealth2016.22 |
| Company DUNS | 042410688 |
| Company Name | CERNER CORPORATION |
| 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 | 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 | false |