Skip to content

DK50 De

by EKOM spol. s r.o. EUDAMED

Active European Union

Ref 430402A09-300Model DK50 DE

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08586014624774 Basic UDI-DIDate25 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Medical compressor
Model / Reference
DK50 DE, 430402A09-300
Primary DI / UDI-DI
08586014624774
Basic UDI-DI
B-08586014624774
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class IIb
Market of Registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000002069

Other devices from EKOM spol. s r.o.

See all devices from EKOM spol. s r.o. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No