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 |