| Primary Device ID | 09120095900274 |
| NIH Device Record Key | 27e111b3-21de-478c-bc64-540e0f58457b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | femSense Ovulation Tracker |
| Version Model Number | 1 |
| Company DUNS | 300492871 |
| Company Name | SteadySense GmbH |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |