| Primary Device ID | 00358962203688 |
| NIH Device Record Key | bc1fb144-d367-4ca1-9a92-78dde781d639 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ScarAway Silicone Scar Sheets |
| Version Model Number | Lot Code |
| Company DUNS | 081138954 |
| Company Name | Alliance Pharma 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |