| Primary Device ID | 10878799002058 |
| NIH Device Record Key | 20076331-8d68-4ce5-a5b8-fa3ce1e81aa6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SURGISTAR, INC. |
| Version Model Number | 121198 |
| Company DUNS | 808865125 |
| Company Name | SURGISTAR, 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 | 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 |