FDA UDI In Commercial Distribution 🇺🇸 United States

KINVENT

DI: 03770011995554 · Model: Sens V2R01 · KINVENT HELLAS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KINVENT
Primary DI
03770011995554
Version / Model
Sens V2R01
Company Name
KINVENT HELLAS
Labeler DUNS
524664525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-01
Public Version
2
Public Version Date
2021-11-30
Public Version Status
Update
Public Device Record Key
51ce64df-960f-4115-8295-f635b36a997d

Device Description

Sens 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 03770011995554

Customer Contacts

Phone
+33467130033

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius