FDA UDI In Commercial Distribution 🇺🇸 United States

MotionSense Digital Goniometer

DI: 55060808320007 · Model: MotionSense 2.0 · ENMOVI LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MotionSense Digital Goniometer
Primary DI
55060808320007
Version / Model
MotionSense 2.0
Catalog Number
007-00036-US
Company Name
ENMOVI LTD
Labeler DUNS
225424353
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-13
Public Version
2
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
64a14eb5-6768-475c-abaf-d8b8eab26a60

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQX Goniometer, Ac-Powered

GMDN Terms

Code Name
33652 Electronic goniometer/kinesiology sensor

Identifiers

Type ID
Primary 55060808320007

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 25 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 75 Percent (%) Relative Humidity