| Primary Device ID | 07640174660032 |
| NIH Device Record Key | 78f8f4c7-9a66-4ec4-8f72-890ec1e40d6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Erigo |
| Version Model Number | Basic |
| Catalog Number | 29564 |
| Company DUNS | 487876203 |
| Company Name | HOCOMA AG |
| 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 | 07640174660032 [Primary] |
| BXB | Exerciser, Powered |
| 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 | 2018-03-29 |
| Device Publish Date | 2016-08-22 |
| 07640174660131 | Basic |
| 07640174660056 | Basic |
| 07640174660032 | Basic |
| 07629999033894 | Pro |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ERIGO 79000906 3050936 Live/Registered |
Hocoma AG 2004-01-22 |
![]() ERIGO 77377607 4099250 Live/Registered |
Erigo Technologies LLC 2008-01-22 |