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EUDAMED last updated this device on May 12, 2026
805663336VF600086VF LASERS VF6000 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by VF SISTEMI ITALIA S.R.L.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08056633360037805663336VF600086VF6000-1200W-808(01)08056633360037
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
X0501HIGH INTENSITY ELECTROMAGNETIC RADIATION EMITTING EQUIPMENT WITHOUT AN INTENDED MEDICAL PURPOSE INTENDED FOR USE ON THE HUMAN BODY, FOR SKIN RESURFACING, TATTOO OR HAIR REMOVAL OR OTHER SKIN TREATMENT – LASER1 warning recorded — scroll inside the panel to see all entries.
CW261No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Austria | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| France | Still on market |
IT-MF-000054326No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.