| Primary Device ID | 00887761982239 |
| NIH Device Record Key | d48ec29f-862f-4df7-8bfc-3874dc2b6975 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HandControl LR |
| Version Model Number | 3126038 |
| 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 | 00887761982239 [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 | 2020-07-10 |
| Device Publish Date | 2020-07-02 |
| 00887761982239 | Overhead track patient lifting/transfer system |
| 00887761982222 | Overhead track patient lifting/transfer system |
| 00887761982215 | Overhead track patient lifting/transfer system |
| 00887761982208 | Overhead track patient lifting/transfer system |
| 00887761974807 | HandControl LR S, ES 2-button |