| Primary Device ID | 00817395021974 |
| NIH Device Record Key | 63e0f936-2fb8-4808-b871-86f409705252 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kennestone Angio |
| Version Model Number | WK100 |
| Company DUNS | 015179820 |
| Company Name | PACKROOM 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 | 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |