| Primary Device ID | 08800118605331 |
| NIH Device Record Key | 7529cf9e-172f-4308-88f1-630e11a7923d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Everest / MegaPlus |
| Version Model Number | D MO A2 20 |
| Company DUNS | 694821663 |
| Company Name | U&C International 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |