| Primary Device ID | 08809524496533 |
| NIH Device Record Key | 63a002c6-2e28-43fb-830b-e84050919f3b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3H |
| Version Model Number | 3h-1370 S12 |
| Company DUNS | 690390383 |
| Company Name | 3H, 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 | true |
| Device Combination Product | false |
| Single Use | false |
| 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 |