| Primary Device ID | 04562122958936 |
| NIH Device Record Key | b3b8e2b8-406a-4c50-89df-85e9ab12052f |
| Commercial Distribution Discontinuation | 2018-03-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | HITACHI, LTD. |
| Version Model Number | UST-5550-R |
| Company DUNS | 693002605 |
| Company Name | HITACHI, LTD. |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |