| Primary Device ID | 00887761983502 |
| NIH Device Record Key | 2b9c152d-796c-4eed-a389-14a5f11127ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Liko Soft Original HighBack Sling™, Mod. 26 |
| Version Model Number | 3526118 |
| Company DUNS | 354818510 |
| Company Name | Liko AB |
| 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 | false |
| Serial Number | true |
| 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 |