FDA UDI In Commercial Distribution 🇺🇸 United States

KForce Sens

DI: 03770011995462 · Model: K Move V3 · KINVENT BIOMECANIQUE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KForce Sens
Primary DI
03770011995462
Version / Model
K Move V3
Company Name
KINVENT BIOMECANIQUE
Labeler DUNS
269560516
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-03
Public Version
1
Public Version Date
2024-01-11
Public Version Status
New
Public Device Record Key
9e68a6c5-c8f1-4e34-920c-5c96daadb081

Device Description

K Move is an inertial sensor to measure the range of motion and to compare the symmetry between the injured limb’s amplitude and the healthy limb.

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
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
No
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 03770011995462

Customer Contacts

Phone
+33467130033

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal