Primary Device ID | 07640174420032 |
NIH Device Record Key | b166062b-875e-47c5-9bb5-0c8b4f2ffa12 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G-EO |
Version Model Number | G-EO |
Company DUNS | 486234078 |
Company Name | Reha Technology 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 | false |
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 | 07640174420032 [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 | 2020-05-06 |
Device Publish Date | 2019-06-02 |
07640174420032 - G-EO | 2020-05-06Robotic-assisted gait trainer |
07640174420032 - G-EO | 2020-05-06 Robotic-assisted gait trainer |
07640174420018 - G-EO System | 2020-05-06 Robotic-assisted gait trainer |
07640174420025 - Armotion | 2018-03-29 Robotic assisted device for the rehabilitation of the upper extremity |