FDA UDI In Commercial Distribution 🇺🇸 United States

KneeKG-Exoskeleton

DI: 00627843933243 · Model: 0 · Emovi Inc
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KneeKG-Exoskeleton
Primary DI
00627843933243
Version / Model
0
Catalog Number
P-080
Company Name
Emovi Inc
Labeler DUNS
247640605
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-18
Public Version
1
Public Version Date
2022-03-28
Public Version Status
New
Public Device Record Key
702b1a4b-92bb-4ba1-84ff-be384c0ac3af

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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

GMDN Terms

Code Name
35757 Gait analysis system

Identifiers

Type ID
Primary 00627843933243