| Primary Device ID | 01618125160975 |
| NIH Device Record Key | ef471908-904a-4318-84ae-e6cd6dbf8f3e |
| Commercial Distribution Discontinuation | 2022-09-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Paramount Medical Solutions |
| Version Model Number | 31432 |
| Company DUNS | 063519193 |
| Company Name | TIDI PRODUCTS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |