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KB50

by Kajo Apuvälineet Oy EUDAMED

Active European Union

Ref KB50 150CB, KB50 250AB, KB50 250CB, KB50 45CBModel KB25 KB50 KB100 KSB80

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6429810721KajoButtonUD Basic UDI-DIDate4 Apr 2022RegisteredStatusActive

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  • Withdrawn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
KajoButton
Model / Reference
KB25 KB50 KB100 KSB80, KB50 150CB, KB50 250AB, KB50 250CB, KB50 45CB
Primary DI / UDI-DI
06429810721129, 06429810721136, 06429810721150, 06429810721204
Basic UDI-DI
6429810721KajoButtonUD
Direct Marketing DI
06429810721129
06429810721136
06429810721150
06429810721204
EMDN Code
Y240999 Control devices and systems - other
Device Class
Class I
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000002471

Other devices from Kajo Apuvälineet Oy

See all devices from Kajo Apuvälineet Oy →

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