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Uniburn After Sun

by Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. EUDAMED

Active European Union

Ref UNIBURN AFTER SUN

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-UNIBURNMD6802BC Basic UDI-DIDate17 Apr 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
UNIBURN AFTER SUN
Primary DI / UDI-DI
D-UNIBURNMD6802BC
Basic UDI-DI
B-UNIBURNMD6802BC
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000032960

Other devices from Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A.

Properties

Show 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