| Primary Device ID | 00810052864785 |
| NIH Device Record Key | b3db1df9-3e25-4e7a-89e2-b575667c394f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Boost 4 Centrifuge, Drucker |
| Version Model Number | 00-289-009-000 |
| Catalog Number | 00-289-009-000 |
| Company DUNS | 022156957 |
| Company Name | DRUCKER DIAGNOSTICS |
| 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 | false |
| Lot Batch | true |
| Serial Number | true |
| 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 |
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