| Primary Device ID | 04719872850250 |
| NIH Device Record Key | 4a1df150-2eaf-4f43-a5b2-faa36793813b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BONASSE |
| Version Model Number | G-90 |
| Company DUNS | 657544912 |
| Company Name | BONASSE ENTERPRISES CO., 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 | true |
| Serial Number | false |
| 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 |