| Primary Device ID | 08809324768427 |
| NIH Device Record Key | c0cdb97c-f5a8-4145-bb51-2b58d67bc35f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | rainbow Block |
| Version Model Number | W9820 |
| Catalog Number | W9820 |
| Company DUNS | 690083006 |
| Company Name | GENOSS CO., Ltd. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |