| Primary Device ID | 90857275007813 |
| NIH Device Record Key | 1a9f9b5e-0893-4235-85f4-95efe3c58e1a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/M |
| Version Model Number | 12511105000034 |
| Company DUNS | 080651010 |
| Company Name | IDUN SOLUTIONS LLC |
| 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 | true |
| 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 | true |