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Base Botuliinitoksiini Ja Kontraindikaatio Dg

by Oy Apotti Ab EUDAMED

Active European Union

Ref OLL0001015 BASE BOTULIINITOKSIINI JA KONTRAINDIKAATIO DG

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-OLL0001015MY Basic UDI-DIDate20 Feb 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  • Withdrawn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

Device Name
Base Botuliinitoksiini Ja Kontraindikaatio Dg
Model / Reference
OLL0001015 BASE BOTULIINITOKSIINI JA KONTRAINDIKAATIO DG
Primary DI / UDI-DI
D-OLL0001015MY
Basic UDI-DI
B-OLL0001015MY
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000007544

Other devices from Oy Apotti Ab

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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