FDA UDI In Commercial Distribution 🇺🇸 United States

Kinesia

DI: 00859584006232 · Model: 502-0268 Kinesia Finger Sleeves · Great Lakes Neurotechnologies Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kinesia
Primary DI
00859584006232
Version / Model
502-0268 Kinesia Finger Sleeves
Catalog Number
502-0268
Company Name
Great Lakes Neurotechnologies Inc.
Labeler DUNS
965540359
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-27
Public Version
2
Public Version Date
2021-03-03
Public Version Status
Update
Public Device Record Key
5cc1e101-2b71-487e-8fd0-96b416048ba2

Device Description

Kinesia Finger Sleeves

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
Has Serial Number
No
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
GYD Transducer, Tremor

GMDN Terms

Code Name
32546 Tremor transducer

Identifiers

Type ID
Primary 00859584006232

Premarket Submissions

Submission Number Supplement Number
K063872 000