| Primary Device ID | 10887761984278 |
| NIH Device Record Key | 3f3514b1-e958-4872-8b1a-9e691bf09700 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Solo RepoSheet™ lift aid |
| Version Model Number | 36871003 |
| 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 | false |
| 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 | 00887761984271 [Primary] |
| GS1 | 10887761984278 [Package] Contains: 00887761984271 Package: [20 Units] In Commercial Distribution |
| 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 | 2021-03-30 |
| Device Publish Date | 2021-03-22 |
| 10887761984278 | Patient lifting system stretcher |
| 00887761976757 | Patient lifting system stretcher |