FDA UDI In Commercial Distribution 🇺🇸 United States

Kinesis QTUG

DI: 05391542950003 · Model: 3.2.2 · KINESIS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kinesis QTUG
Primary DI
05391542950003
Version / Model
3.2.2
Company Name
KINESIS
Labeler DUNS
985574496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-22
Public Version
1
Public Version Date
2023-03-02
Public Version Status
New
Public Device Record Key
a4ed5358-2d49-4cf8-b9c6-cd97561e70c7

Device Description

QTUG consists of a device for assessment of mobility, falls risk and frailty in older adults through quantitative analysis of movement using body-worn inertial sensors. The device streams data over a Bluetooth interface to an Android tablet device.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PJP Fall Prevention Alarm/Sensor Attached Only

GMDN Terms

Code Name
35757 Gait analysis system

Identifiers

Type ID
Primary 05391542950003