| Primary Device ID | 07290013820280 |
| NIH Device Record Key | 656a0273-3401-4397-ab65-e6f2a9406d4a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DSI |
| Version Model Number | PSGS-T-4 |
| Company DUNS | 023572393 |
| Company Name | SLP 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 | true |
| 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 |