| Primary Device ID | 07290013820273 |
| NIH Device Record Key | 31503ff0-9456-40af-83c7-31ec07a24533 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DSI |
| Version Model Number | PSGA-T-4P |
| 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 |