FDA UDI In Commercial Distribution 🇺🇸 United States

EVRF

DI: 05425025630080 · Model: 00EVRFV2 · F Care Systems
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVRF
Primary DI
05425025630080
Version / Model
00EVRFV2
Company Name
F Care Systems
Labeler DUNS
370516974
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-08
Public Version
1
Public Version Date
2026-04-16
Public Version Status
New
Public Device Record Key
b24fe3b3-b260-4f17-a5b6-b62c4dead83a

Device Description

Intended for the epilation and for the treatment of lower limb spider vein or telangiectasia by thermocoagulation

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
ONQ Electrosurgical Coagulation For Aesthetic

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 05425025630080

Customer Contacts

Phone
+3234515145

Premarket Submissions

Submission Number Supplement Number
K130283 000