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Delphic

by Davis Schottlander & Davis Ltd 168 variants

Ref 0766:04:07Model Delphic Anterior Denture Teeth, Acrylic Teeth

Active European Union

CE MDR CE MDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-05052674069949 Basic UDI-DI 05052674069949UDI-DIDate28 Apr 2026RegisteredStatusActive
European UnionCE/MDD NumberB-05052674069949 Basic UDI-DI 05052674069949UDI-DIDate28 Apr 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  • Withdrawn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, CE/MDD Active

Specification

EUDAMED

Device Name
0766:04:07
Teeth
Model / Reference
Delphic Anterior Denture Teeth, 0766:04:07, Acrylic Teeth
Primary DI / UDI-DI
05052674069949
Basic UDI-DI
B-05052674069949, 5052674TEETH-CL1AZ
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class I
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000035008
Authorised representative
Schottlander (IRL) Ltd IE-AR-000029625

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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