| Primary Device ID | 10850015055611 |
| NIH Device Record Key | 34e4f286-ec65-426b-9c46-357e428ceb3a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BLEEDING CONTROL TREATMENT PACK |
| Version Model Number | S-25618 |
| Company DUNS | 039612668 |
| Company Name | ULINE, INC. |
| 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 | true |
| 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 |