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Intraoral Scanner

by Liaoning Upcera Co Ltd 7 variants

Ref /Model Intraoral Scanner

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 Number694138229906HM Basic UDI-DI 06941382285583UDI-DIDate12 Aug 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Intraoral Scanner
Model / Reference
Intraoral Scanner, /
Primary DI / UDI-DI
06941382285583
Basic UDI-DI
694138229906HM
Direct Marketing DI
06941382285583
EMDN Code
Z11030402 Systems for intraoral digital videoradiography
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000013088
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Liaoning Upcera Co., Ltd.

See all devices from Liaoning Upcera Co., Ltd. →

Properties

Other properties (13)

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