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Oktagon

by Hager & Meisinger GmbH 37 variants

Ref 31176Model Oktagon Dental Implants

Active European Union

CE MDR

Valid until

6 Mar 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV NORD CERT GmbH

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/MDR Number++E0HM250IIB02AA34 Basic UDI-DIDate23 Jul 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 44911220651 Active Supplemented

    Quality management system EU MDR

    Notified body
    TÜV NORD CERT GmbH 0044
    Issued
    12 Aug 2025
    Expires
    6 Mar 2029
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Oktagon Dental Implants, 31176
Primary DI / UDI-DI
E0HM311761
Basic UDI-DI
++E0HM250IIB02AA34
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004966

Other devices from Hager & Meisinger GmbH

See all devices from Hager & Meisinger GmbH →

Properties

  • Sterile
  • Implantable
  • Sutures

Other properties (11)

  • 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