| Primary Device ID | 08800118611257 |
| NIH Device Record Key | 294ff3d7-939b-4bd8-9ec4-5fff8d3e7589 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Everest |
| Version Model Number | W MO A1 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800118611257 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-24 |
| Device Publish Date | 2022-02-16 |