| Primary Device ID | 30641043810525 |
| NIH Device Record Key | 7c254dc4-779e-435a-b741-2e98410df8ac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nut and Gland |
| Version Model Number | 10-810-52 |
| Company DUNS | 032705659 |
| Company Name | MERCURY ENTERPRISES, INC. |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |