FDA UDI In Commercial Distribution 🇺🇸 United States

K Myo

DI: 03770011995707 · Model: K Myo V3 · KINVENT BIOMECANIQUE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K Myo
Primary DI
03770011995707
Version / Model
K Myo V3
Company Name
KINVENT BIOMECANIQUE
Labeler DUNS
269560516
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-05
Public Version
1
Public Version Date
2024-01-15
Public Version Status
New
Public Device Record Key
5d9b7107-0556-4cc6-9801-a07f1c557181

Device Description

K Myo is a biofeedback device for training muscle groups by means of electromyography

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
HCC Device, Biofeedback

GMDN Terms

Code Name
11474 Electromyograph

Identifiers

Type ID
Primary 03770011995707

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