| Primary Device ID | 07290017844107 |
| NIH Device Record Key | 8877a4e7-6278-41a3-a9ba-2456c7e87247 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REOGO |
| Version Model Number | 08 |
| Catalog Number | REOGO005SYS |
| Company DUNS | 534078621 |
| Company Name | MOTORIKA MEDICAL (ISRAEL) LTD |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290017844107 [Primary] |
| IKK | System, Isokinetic Testing And Evaluation |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-08-05 |
| Device Publish Date | 2019-05-31 |
| 07290017844114 | The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients wit |
| 07290017844107 | The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients wit |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REOGO 77068129 3513149 Live/Registered |
Motorika Limited 2006-12-20 |