| Primary Device ID | M9831108000021 |
| NIH Device Record Key | 11f23fb4-7771-4823-abbb-cbe6e9790839 |
| Commercial Distribution Discontinuation | 2018-08-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Mespere |
| Version Model Number | IFU-V2000 |
| Company DUNS | 203147665 |
| Company Name | Mespere LifeSciences Inc |
| 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 | true |
| 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 |