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REVOFIL Fine

by Caregen Co., Ltd. EUDAMED

Active European Union

Model REVOFIL Fine

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809171383941 Basic UDI-DIDate27 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Soft Touch Filler
Model / Reference
REVOFIL Fine
Primary DI / UDI-DI
08809171383941
Basic UDI-DI
B-08809171383941
EMDN Code
Y062703 Aesthetic fillers, calf and thigh
Device Class
Class III
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
KR-MF-000009948
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Caregen Co., Ltd.

See all devices from Caregen Co., Ltd. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • 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