| Primary Device ID | 10887761979595 |
| NIH Device Record Key | 201fb4b4-7fdd-4183-8fdc-209220088170 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FixStrap™ |
| Version Model Number | 3696002 |
| 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 | 00887761979598 [Primary] |
| GS1 | 10887761979595 [Package] Contains: 00887761979598 Package: [10 Units] In Commercial Distribution |
| FSA | Lift, patient, non-ac-powered |
| IKX | AID, TRANSFER |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-03-31 |
| Device Publish Date | 2021-03-23 |
| 10887761983455 | General-purpose patient lifting system sling/harness |
| 10887761979595 | Patient transfer sliding mat |