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Algyl CBD náplast na bolest

by Cannordic a/S EUDAMED

Active European Union

Ref PL-CSPP100307

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number574400013MDPAIP21FT Basic UDI-DIDate12 Mar 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Pain Patch
Model / Reference
PL-CSPP100307
Primary DI / UDI-DI
08594060120966
Basic UDI-DI
574400013MDPAIP21FT
Direct Marketing DI
08594060120966
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
DK-MF-000003852

Other devices from Cannordic A/S

See all devices from Cannordic A/S →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No