Skip to content

LaCorium, Dermal Therapy Fungistop Camouflage 4ml ANZ

by Medical Brands Developments BV

Ref 4NBN.LAC.ANZModel Fungal Nail Treatment

Active European Union

CE MDR

Valid until

20 Dec 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Eurofins Product Testing Italy S.r.l.

Trust

Unverified

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

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number872064894020HA Basic UDI-DI 09329224004573UDI-DIDate22 May 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.25/5701 Active

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    21 Jan 2025
    Expires
    20 Dec 2027

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Fungal Nail Treatment, 4NBN.LAC.ANZ
Primary DI / UDI-DI
09329224004573
Basic UDI-DI
872064894020HA
EMDN Code
M0410 Dressings for nails in the form of liquids, gels and creams
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
NL-MF-000002672

Other devices from Medical Brands Developments BV

See all devices from Medical Brands Developments BV →

Properties

Other properties (13)

  • 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