| Primary Device ID | 00747252031443 |
| NIH Device Record Key | 6ab247a2-c5c2-4560-a0fa-df1286705cd0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Superior Products Inc |
| Version Model Number | MFY-973-4 |
| Company DUNS | 078607495 |
| Company Name | Superior Products, LLC |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |