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SLH DC Temporary Gingiva Former

by SLH Microtech GmbH EUDAMED

Active European Union

Ref DC 32034Model DC Superstructures

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2616701 Date16 Jun 2026IssuedStatusActive expires 15 Jun 2031
European UnionCE/MDD NumberB-04260662231525 Basic UDI-DIDate3 Nov 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Certificates

1 certificate · EUDAMED

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

    Quality management system EU MDR

    Notified body
    2975
    Issued
    16 Jun 2026
    Expires
    15 Jun 2031

Specification

EUDAMED

Trade Name
SLH DC Temporary Gingiva Former
Temporary Gingiva Former Ø 6.0 mm Peek
Device Name
Temporary Gingiva Former
Model / Reference
DC 32034, DC Superstructures
Primary DI / UDI-DI
04260662231525
Basic UDI-DI
B-04260662231525, 426066223TGFG4
Direct Marketing DI
04260662231525
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
Market of Registration
Germany

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