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DuraCetal

by The Myerson Company Limited 18 variants

Ref DC-DISC-A5-9820

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08423261ThermoplasticDR5S Basic UDI-DI 00842326104501UDI-DIDate8 Mar 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  • Withdrawn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

Device Name
Thermoplastic denture base resin
Model / Reference
DC-DISC-A5-9820
Primary DI / UDI-DI
00842326104501
Basic UDI-DI
08423261ThermoplasticDR5S
EMDN Code
Q0102050102 Dental rebasing resins
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
TT-MF-000045141
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from The Myerson Company Limited

See all devices from The Myerson Company Limited →

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