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PANNORAMIC 250 Flash III DX Digital Scanner

by 3DHISTECH Kft. 5 variants

Ref DX-02503-F1204ACBAModel PANNORAMIC 250 Flash III DX Digital Scanner

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5999571470266JC Basic UDI-DI 05999571470181UDI-DIDate13 Jan 2023RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
PANNORAMIC 250 Flash III DX Digital Scanner, DX-02503-F1204ACBA
Primary DI / UDI-DI
05999571470181
Basic UDI-DI
5999571470266JC
Direct Marketing DI
05999571470181
EMDN Code
W0202050304 Digital laboratory microscopes
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
HU-MF-000014337

From the manufacturer

Manufacturer's product page: Pannoramic 150 Digital Scanner

Other devices from 3DHISTECH Kft.

See all devices from 3DHISTECH Kft. →

Properties

  • Professional Testing
  • Surgical Instrument

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • New Device: No