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AnyHand

by LIME medical GmbH 3 variants

Ref 4260667450174

Active European Union

CE MDR

Valid until

1 Apr 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000324421 Date27 Aug 2026IssuedStatusActive expires 1 Apr 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000324421 Active Supplemented

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    27 Aug 2026
    Expires
    1 Apr 2031
    Reason
    Change approved

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
AnyHand
Model / Reference
4260667450174
Primary DI / UDI-DI
42606674501742
Basic UDI-DI
426066745AnyHandMDR6E
Direct Marketing DI
42606674501742
EMDN Code
Z120616 Electromechanical systems for physical therapy
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000015593

Other devices from LIME medical GmbH

  • AnyHand

    Class IIa

  • AnyHand

    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