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Intuy Knee NEO

by Reboocon Bionics B.V. EUDAMED

Active European Union

Ref IK1N

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number24M00080CRT05 Date23 Oct 2025IssuedStatusActive expires 2 Dec 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 24M00080CRT05 Amended

    Quality management system EU MDR

    Notified body
    Notified body 1912
    Issued
    23 Oct 2025
    Expires
    2 Dec 2029
    Reason
    Other

Specification

EUDAMED

Device Name
Intuy Knee
Model / Reference
IK1N
Primary DI / UDI-DI
08720299459830
Basic UDI-DI
87202994598ILK98
EMDN Code
Y062412,Y062415
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
NL-MF-000000239

From the manufacturer

Manufacturer's product page: Intuy® Knee

Other devices from Reboocon Bionics B.V.

  • Intuy Knee PRO

    Class IIa

  • Intuy Knee RISE

    Class IIa

  • Intuy Knee

    Class IIa

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