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Delta 30 UV Ultimate

by HEINE Optotechnik GmbH & Co. KG

Ref K-242.28.212

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4053755_D-S_19_YT Basic UDI-DI 04053755212934UDI-DIDate1 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
K-242.28.212
Primary DI / UDI-DI
04053755212934
Basic UDI-DI
4053755_D-S_19_YT
EMDN Code
Z12040108 Dermatoscopes
Device Class
Class I
Medical Purpose
This is a collection of devices intended for use by physicians to help them perform skin examinations on patients.

Manufacturer details

EUDAMED SRN
DE-PR-000035500

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Properties

Other properties (1)

  • Sterile: No