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DK50

by EKOM spol. s r.o. 4 variants

Ref 401402001-002Model DK50

DK50 (401402001-002) is a Class IIa device made by EKOM spol. s r.o., registered in EUDAMED on 9 Jun 2026 (Basic UDI-DI 858601462000002KX), active as of 22 Oct 2026.

Active European Union

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number858601462000002KX Basic UDI-DI 08586014622022UDI-DIDate9 Jun 2026RegisteredStatusActive
European UnionCE/MDR Number858601462000002KX Basic UDI-DI 08586014622022UDI-DIDate9 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Dental Compressors
Dental compressor
Model / reference
401402001-002, DK50
Primary DI / UDI-DI
08586014622022
Basic UDI-DI
858601462000002KX, B-08586014622022
Direct marketing DI
08586014622022
EMDN code
Q0199 Odontology devices - other
Device class
Class IIa
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000002069

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

Other devices from EKOM spol. s r.o.

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

Properties

Other properties (14, all answered No)