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Xerf Effector 40(300)

by Cynosure Lutronic Technology Corporation

Ref XERF EFFECTOR 40(300)Model XERF EFFECTOR 40(300), XERF EFFECTOR 40(600), XERF EFFECTOR 40(900), XERF EFFECTOR 60(600), XERF EFFECTOR 60(900), XERF EFFECTOR 60(1200)

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number88002918211011BGX Basic UDI-DI 08800291821429UDI-DIDate22 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08800291821429 UDI-DI Date8 Apr 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Xerf Effector 40(300) EUDAMED
Xerf GUDID
Generic Name
Radio-frequency skin/body contouring system
Device Name
Electrosurgical electrode
Model / Reference
XERF EFFECTOR 40(300), XERF EFFECTOR 40(600), XERF EFFECTOR 40(900), XERF EFFECTOR 60(600), XERF EFFECTOR 60(900), XERF EFFECTOR 60(1200)
Primary DI / UDI-DI
08800291821429
Basic UDI-DI
88002918211011BGX
FDA Product Code
GEI
EMDN Code
X0599 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
GMDN Term
Radio-frequency skin/body contouring system
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
878.4400
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

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Properties

  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No