| Primary Device ID | 00840763100087 |
| NIH Device Record Key | ad5a6509-3178-4f2e-9fcb-705d000ac0f5 |
| Commercial Distribution Discontinuation | 2016-12-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Cellfina Prep Pack for EU |
| Version Model Number | CP1 Rev B |
| Company DUNS | 010981554 |
| Company Name | ULTHERA, INC. |
| 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 | 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 |