| Primary Device ID | M9831107000031 |
| NIH Device Record Key | 41ac071c-ca88-4d3f-bc0e-79b6ae0a42b9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mespere |
| Version Model Number | SRA-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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |