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Dr. Scholl's Freeze Away MAX Verruca & Wart Remover

by Pronova Laboratories BV

Ref FW10UKAU100Model FW10XX100

Active European Union

CE MDR

Valid until

1 Dec 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DEKRA Certification B.V.

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 Number2260052CE01 Date21 Oct 2026IssuedStatusActive EUDAMED: not on the EU market expires 1 Dec 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2260052CE01 Active Supplemented

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    21 Oct 2026
    Expires
    1 Dec 2028
    Reason
    Change approved

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Forwarts Wart Remover
Model / Reference
FW10XX100, FW10UKAU100
Primary DI / UDI-DI
08717344390576
Basic UDI-DI
871734439FW10XXJ9
Direct Marketing DI
08717344390576
EMDN Code
V0999 Fluids/gases for clinical/therapeutical use - other
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
NL-MF-000001486

Other devices from Pronova Laboratories BV

See all devices from Pronova Laboratories 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