| Primary Device ID | 00887761983281 |
| NIH Device Record Key | 0197226e-20e8-4199-92c7-ffd8b6e7fcc3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Liko Original HighBack Sling™, Mod. 210 |
| Version Model Number | 35210115 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887761983281 [Primary] |
| FSA | Lift, patient, non-ac-powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2020-06-15 |
| 00887761983335 | Patient lifting system divided leg sling |
| 00887761983328 | Patient lifting system divided leg sling |
| 00887761983304 | Patient lifting system divided leg sling |
| 00887761983281 | Patient lifting system divided leg sling |
| 00887761983274 | Patient lifting system divided leg sling |
| 00887761983311 | Patient lifting system divided leg sling |
| 00887761983298 | Patient lifting system divided leg sling |