FDA UDI In Commercial Distribution 🇺🇸 United States

REOGO

DI: 07290017844107 · Model: 08 · MOTORIKA MEDICAL (ISRAEL) LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REOGO
Primary DI
07290017844107
Version / Model
08
Catalog Number
REOGO005SYS
Company Name
MOTORIKA MEDICAL (ISRAEL) LTD
Labeler DUNS
534078621
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-31
Public Version
2
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
8877a4e7-6278-41a3-a9ba-2456c7e87247

Device Description

The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKK System, Isokinetic Testing And Evaluation

GMDN Terms

Code Name
47517 Virtual-display rehabilitation system, powered-support, upper-limb

Identifiers

Type ID
Primary 07290017844107