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Clinik Des Al

by KIMI d.o.o., proizvodno trgovsko podjetje 3 variants

Ref 10594Model 1L

Active European Union

CE MDR

Valid until

24 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SLOVENIAN INSTITUTE OF QUALITY AND METROLOGY - SIQ

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number383007329AlDesEF Basic UDI-DI Date29 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
10594, 1L
Primary DI / UDI-DI
03830073295358, 03830000218764
Basic UDI-DI
383007329AlDesEF, B-03830000218764
EMDN Code
D0799 Alcohols for the disinfection of medical devices - other
Device Class
Class IIa
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000029067

Other devices from KIMI d.o.o., proizvodno trgovsko podjetje

  • Clinik Des Al

    Class IIa

  • Clinik Des Al

    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