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Spider Kp (Ss)

by SteelBo Sp.z o.o. Poland EUDAMED

Ref SPIDER KP (SS)

EMDN Y062499

Regulatory status

as of 25 Oct 2026

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

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Adaptery do laminacji leja
Model / Reference
SPIDER KP (SS)
Primary DI / UDI-DI
05905601771838
Basic UDI-DI
5905601771LAMADAPTER5T
EMDN Code
Y062499 Lower extremity prostheses - other
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000037622

Other devices from SteelBo Sp.z o.o.

See all devices from SteelBo Sp.z o.o. →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 01db58dc-c56a-4c5e-b899-df45f396e07e 61 fields · synced 25 Oct 2026