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Spider Kc (Ti)

by SteelBo Sp.z o.o. EUDAMED

Active European Union

Ref SPIDER KC (TI)

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5905601771LAMADAPTER5T Basic UDI-DIDate25 May 2026RegisteredStatusActive

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  • Withdrawn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
Adaptery do laminacji leja
Model / Reference
SPIDER KC (TI)
Primary DI / UDI-DI
05901247378219
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000037622

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