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DK50 2VS

by EKOM spol. s r.o. 11 variants

Part of a family of 329 devices: see the family page

Ref 403202001-307Model DK50 2VS

DK50 2VS (403202001-307) is a Class IIa device made by EKOM spol. s r.o., registered in EUDAMED on 18 Jun 2026 (Basic UDI-DI B-08586014623005), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-08586014623005 Basic UDI-DI 08586014623005UDI-DIDate18 Jun 2026RegisteredStatusActive
European UnionCE/MDD NumberB-08586014623005 Basic UDI-DI 08586014623005UDI-DIDate18 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Specification

EUDAMED

Device name
Dental compressor
Dental Compressors
Model / reference
DK50 2VS, 403202001-307
Primary DI / UDI-DI
08586014623005
Basic UDI-DI
B-08586014623005, 858601462000002KX
Direct marketing DI
08586014623005
EMDN code
Q0199 Odontology devices - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
Standard device
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)