| Primary Device ID | 08809520341110 |
| NIH Device Record Key | f7667cd0-e975-49af-8fe1-6531e42b3f0b |
| Commercial Distribution Discontinuation | 2023-03-17 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | OLZ-200 |
| Version Model Number | OLZ-200 FACE MASK |
| Company DUNS | 689458057 |
| Company Name | GTG Wellness Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Serial Number | true |
| 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 |