FDA UDI In Commercial Distribution 🇺🇸 United States

MotionSense Adhesive Refill Kit

DI: 15060808320108 · Model: 007-00067-US · ENMOVI LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MotionSense Adhesive Refill Kit
Primary DI
15060808320108
Version / Model
007-00067-US
Catalog Number
007-00067-US
Company Name
ENMOVI LTD
Labeler DUNS
225424353
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-15
Public Version
2
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
827cab3d-8a9b-4ea7-838e-e6cf76ef2d32

Device Description

MotionSense Adhesive Refill Kit

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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 15060808320108

Storage Conditions

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