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Bliznoxin

by LABORATOIRE L'IDEAL Parisien Sp. z o.o. EUDAMED

Active European Union

Ref BLIZNOXIN Scar gel 20ml tube in a carton with instructions for use. Polish language version.Model BLIZNOXIN Scar gel 20ml tube in a carton with instructions for use. Polish language version.

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05908226260664 Basic UDI-DIDate6 May 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  • Withdrawn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
Scar gel / Żel na blizny
Model / Reference
BLIZNOXIN Scar gel 20ml tube in a carton with instructions for use. Polish language version.
Primary DI / UDI-DI
05908226260664
Basic UDI-DI
B-05908226260664
EMDN Code
M9002 Protective devices, lubricants and soothing devices (sprays, gels, fluids and creams)
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000005402

Other devices from LABORATOIRE L'IDEAL Parisien Sp. z o.o.

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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