| Primary Device ID | 04041925006315 |
| NIH Device Record Key | 06ef24cf-a82c-4caf-affb-9dd8d3c1f7b3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OmniCycle® Revo |
| Version Model Number | 01.05.ZZ |
| Company DUNS | 328011325 |
| Company Name | medica - Medizintechnik GmbH |
| 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 | 04041925006315 [Primary] |
| BXB | Exerciser, 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 | 2025-12-24 |
| Device Publish Date | 2025-12-16 |
| 04041925006315 | General Description: The system is a therapeutic device for circular passive, assistive or activ |
| 04041925006308 | General Description: The system is a therapeutic device for circular passive, assistive or activ |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OMNICYCLE 77113842 3463332 Live/Registered |
ACCELERATED CARE PLUS CORP. 2007-02-22 |