FDA UDI In Commercial Distribution 🇺🇸 United States

Venus Versa

DI: 07290016540383 · Model: VE102407 · VENUS CONCEPT LTD
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Venus Versa
Primary DI
07290016540383
Version / Model
VE102407
Company Name
VENUS CONCEPT LTD
Labeler DUNS
533127663
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2018-11-21
Public Version Status
Update
Public Device Record Key
cb38785a-6a59-4461-8c0b-6822c2c6380c

Device Description

The Venus Versa system is a multi-application device intended to be used in aesthetic and cosmetic procedures.

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45223 Multi-modality skin surface treatment system generator

Identifiers

Type ID
Package 07290016540499
Primary 07290016540383