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DURADENT - DURACRYL HEAT-CURE Isı ile sertleşen protez kaide materyali Akrilk toz 50kg

by Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇.

Ref yok

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699197589164 Basic UDI-DI 08699197589164UDI-DIDate11 Jun 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
DURACRYL HEAT-CURE Isı ile sertleşen protez kaide materyali Akrilk toz 50kg
Model / Reference
yok
Primary DI / UDI-DI
08699197589164
Basic UDI-DI
B-08699197589164
EMDN Code
Q010299 Prosthetic dentistry devices - other
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000038674

Other devices from Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇.

See all devices from Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇. →

Properties

Other properties (11)

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