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DC 12.5 Press-Correction Material Interface 2

by Estetic Ceram AG

Ref 38-5013

DC 12.5 Press-Correction Material Interface 2 (38-5013) is a Class IIa device made by Estetic Ceram AG, registered in EUDAMED on 1 Apr 2026 (Basic UDI-DI 7630503100007H), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7630503100007H Basic UDI-DI 07630503120283UDI-DIDate1 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Dentalkeramik
Model / reference
38-5013
Primary DI / UDI-DI
07630503120283
Basic UDI-DI
7630503100007H
Direct marketing DI
07630503120283
EMDN code
Q010199 Conservative dentistry and endodontics devices - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
LI-MF-000001476

Similar devices in this category

Other devices filed under CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER.

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Properties

  • Implantable
Other properties (13, all answered No)