| Primary Device ID | 30850015055448 |
| NIH Device Record Key | 869a8c8c-f88f-4060-94ab-a4d37f1fa05e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Knuckle Bandage |
| Version Model Number | S-18571 |
| Company DUNS | 039612668 |
| Company Name | ULINE, INC. |
| Device Count | 50 |
| 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 | 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 |