FDA UDI In Commercial Distribution 🇺🇸 United States

DEKA SIMON

DI: 08057017760696 · Model: M134B1 · DEKA M.E.L.A. SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
DEKA SIMON
Primary DI
08057017760696
Version / Model
M134B1
Catalog Number
M134B1
Company Name
DEKA M.E.L.A. SRL
Labeler DUNS
629381096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-11
Public Version
1
Public Version Date
2023-10-19
Public Version Status
New
Public Device Record Key
0ee4a9d7-fce3-4253-9e83-089f567c9c31

Device Description

The DEKA SIMON is a device provided with 4 handpieces by 2 electrodes each intended to employ EMS (Electrical Muscle Stimulation) technology for various medical application.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 08057017760696

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Handling Environment Temperature
Temperature Range
10 – 35 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 1060 KiloPascal