FDA UDI In Commercial Distribution 🇺🇸 United States

MiniFX

DI: 07290016633238 · Model: AG604696A · INMODE M.D LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MiniFX
Primary DI
07290016633238
Version / Model
AG604696A
Catalog Number
AG604696A
Company Name
INMODE M.D LTD
Labeler DUNS
600417351
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-25
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ce8d8227-62cf-468e-9475-182faf0c5136

Device Description

MiniFX

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
Yes
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
GEI Electrosurgical, Cutting & Coagulation & Accessories
PBX Massager, Vacuum, Radio Frequency Induced Heat

GMDN Terms

Code Name
58454 Radio-frequency skin surface treatment system

Identifiers

Type ID
Primary 07290016633238

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160329 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 65 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 80 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 110 KiloPascal
Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 80 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
90 – 110 KiloPascal