Kinesia 360

GUDID 00859584006072

Tremor transducer

Primary Device ID	00859584006072
NIH Device Record Key	3626c49f-9a0e-4454-985f-04aecde03776
Commercial Distribution Status	In Commercial Distribution
Brand Name	Kinesia 360
Version Model Number	502-0264, Sensor Upper
Company DUNS	965540359
Company Name	GREAT LAKES NEUROTECHNOLOGIES INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	00859584006072 [Primary]

GYD	Transducer, Tremor

Steralize Prior To Use	false
Device Is Sterile	false

00859584006270	Kinesia 360 Flex system is intended to monitor physical motion and muscle activity to quantify k
00859584006263	Kinesia 360 Tablet
00859584006256	Kinesia 360 System
00859584006171	Kinesia 360 Support Application Software
00859584006126	Kinesia 360, Application Software
00859584006089	Kinesia 360, Sensor Lower
00859584006072	Kinesia 360, Sensor Upper
00859584006065	Kinesia 360, Tablet Assembly, Samsung Galaxy
00859584006058	Kinesia 360, Samsung Galaxy Tablet