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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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VF6000 Laser Hair Removal System — 4 UDI-DI variants, MDR

MD Atlas
VF SISTEMI ITALIA S.R.L.

Data from EUDAMED, last updated May 31, 2026

VF6000 Laser Hair Removal System

805663336VF600086

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: VF SISTEMI ITALIA S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805663336VF600086
Device name: VF6000 Laser Hair Removal System
Device model: VF6000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: VF SISTEMI ITALIA S.R.L.
SRN: IT-MF-000054326
Country: Italy
Email: info@vflasers.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRE1CRSMM9FD7ZD6KC8HXESM

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

VF LASERS VF600008056633360037
VF LASERS VF600008056633360013
VF LASERS VF600008056633360020
VF LASERS VF600008056633360006