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Nucleoss T6 Ti-Base Abutment (Cad-Cam Cerec) Ø 4.5 mm

by Sanlilar Tibbi Cihazlar Med. Kim. San. ve Tic. A.Ş.

Ref T6 32802

Active European Union

CE MDR

Valid until

23 Oct 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SZUTEST Konformitätsbewertungsstelle GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2529701 Date8 Jul 2026IssuedStatusActive expires 23 Oct 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2529701 Active Amended

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    8 Jul 2026
    Expires
    23 Oct 2030
    Reason
    Mnf data change

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Nucleoss Cad-Cam Cerec Ti-Base Abutment
Model / Reference
T6 32802
Primary DI / UDI-DI
08699383355221
Basic UDI-DI
869938335CCTATM
Direct Marketing DI
08699383355221
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000014938

Other devices from Sanlilar Tibbi Cihazlar Med. Kim. San. ve Tic. A.Ş.

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Properties

  • Implantable
  • Sutures

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