| Primary Device ID | 04540217051984 |
| NIH Device Record Key | 586ebaf9-e676-4349-a97f-d9b73ec5c001 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FH-21HR |
| Version Model Number | 503-43000-69 |
| Company DUNS | 690558747 |
| Company Name | SHIMADZU CORPORATION |
| 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 | 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 | false |
| OTC Over-The-Counter | false |