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Abilar® Nail Fungal Treatment

by Repolar Pharmaceuticals Oy

Ref 9010Model 30%

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FIMF0000005899010LL Basic UDI-DI D-FIMF0000005899010LLUDI-DIDate9 Nov 2021RegisteredStatusActive

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

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Resin lacquer
Model / Reference
30%, 9010
Primary DI / UDI-DI
D-FIMF0000005899010LL
Basic UDI-DI
B-FIMF0000005899010LL
EMDN Code
M0410 Dressings for nails in the form of liquids, gels and creams
Device Class
Class IIa
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000000589

From the manufacturer

Manufacturer's product page: Abilar® Wound Balm | For wound treatment

Other devices from Repolar Pharmaceuticals Oy

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No