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Venus Versa VE102407

by Venus Concept Inc.

Ref VE102407

Venus Versa VE102407 is a device classified as Class IIb in the EU and Class II in the US made by Venus Concept Inc., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-00810060830680) and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 00810060830680), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00810060830680 Basic UDI-DI 00810060830680UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810060830680 UDI-DI Date8 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00810060830680 registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 00810060830680 listed 8 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810060830680
  2. Registered EUDAMED B-00810060830680

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Venus Versa
Generic name
Multi-modality skin surface treatment system
Model / reference
VE102407
Primary DI / UDI-DI
00810060830680
Basic UDI-DI
B-00810060830680
FDA product code
ONF, GEI
EMDN code
X0502, X0599
GMDN term
Multi-modality skin surface treatment system
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.4810, 878.4400
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Multi-modality skin surface treatment systemRadio-frequency skin/body contouring systemRadio-frequency skin surface treatment system applicator

Similar devices in this category

Other devices filed under HIGH 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.

Other devices from Venus Concept Inc.

See all devices from Venus Concept Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)