| Primary Device ID | 00878953000220 |
| NIH Device Record Key | d0f8e8ed-9e97-4990-b5bb-13f3a10d82fc |
| Commercial Distribution Discontinuation | 2019-01-23 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Aura XP |
| Version Model Number | 0010-8118 |
| 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 | 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 | true |
| OTC Over-The-Counter | false |