Primary Device ID | 07640174660131 |
NIH Device Record Key | 8a5a7429-ddd3-452d-9888-3ae384c19ed7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Erigo |
Version Model Number | Basic |
Catalog Number | 30076 |
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 | 07640174660131 [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 | 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 |