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SLH DC Multi Unit Abut. 0° Ø 4.8 mm H: 2.5 mm

by SLH Microtech GmbH

Ref DC 32423Model DC Superstructures

Active European Union

CE MDR

Valid until

15 Jun 2031

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-2616701 Date16 Jun 2026IssuedStatusActive expires 15 Jun 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2616701 Active

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    16 Jun 2026
    Expires
    15 Jun 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
SLH DC Multi Unit Abutment
Model / Reference
DC Superstructures, DC 32423
Primary DI / UDI-DI
04260662231594
Basic UDI-DI
426066223MAQ3
Direct Marketing DI
04260662231594
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
DE-MF-000020864

Other devices from SLH Microtech GmbH

See all devices from SLH Microtech GmbH →

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