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Denture Gingiva Pro Multistratum

by Zirkonzahn SRL

Ref DSCExx(x)yy(ww)(zzz(z))

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++D800RES001001HB Basic UDI-DI D800DSCExx(x)yy(ww)(zzz(z))0UDI-DIDate18 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Dental Resins
Model / Reference
DSCExx(x)yy(ww)(zzz(z))
Primary DI / UDI-DI
D800DSCExx(x)yy(ww)(zzz(z))0
Basic UDI-DI
++D800RES001001HB
Direct Marketing DI
D800DSCExx(x)yy(ww)(zzz(z))0
EMDN Code
Q01020605 Temporary dental prostheses
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000028795

Related devices

Category: Temporary dental crown/bridge

Other devices from Zirkonzahn SRL

See all devices from Zirkonzahn SRL →

Properties

  • Implantable

Other properties (12)

  • Sterile: 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