| Primary Device ID | 00887761981768 |
| NIH Device Record Key | 6f00dd6f-4fe9-4ddd-993a-b47c96d93046 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Golvo™ mobile lift |
| Version Model Number | 2000049CN |
| 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 | 00887761981768 [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 | 2020-06-17 |
| Device Publish Date | 2020-06-09 |
| 00887761981768 | Mobile patient lifting system, battery-powered |
| 00887761981744 | Mobile patient lifting system, battery-powered |
| 00887761981737 | Mobile patient lifting system, battery-powered |
| 00887761981751 | Mobile patient lifting system, battery-powered |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GOLVO 77641345 3788261 Live/Registered |
LIKO RESEARCH & DEVELOPMENT AB 2008-12-30 |