| Primary Device ID | 00878953009360 |
| NIH Device Record Key | e97e0211-f8d2-4a40-907c-27e76569f837 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aura XP |
| Version Model Number | 1016959-01 |
| Company DUNS | 796308653 |
| Company Name | AMERICAN MEDICAL SYSTEMS |
| 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 | false |
| 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 |