| Primary Device ID | 05420028702109 |
| NIH Device Record Key | f2f7792c-030c-4050-aa6f-ea752a9954b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Orfit Industries |
| Version Model Number | 25000/16/MR |
| Company DUNS | 283679900 |
| Company Name | Orfit Industries NV |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |