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Dental Treatment Units

by KaVo Dental GmbH 7 variants

Ref 1.010.7050

Active European Union

CE MDR

Valid until

28 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DEKRA Certification GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number51512-60-01-00 Date1 Sep 2026IssuedStatusActive expires 28 Sep 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 51512-60-01-00 Active Reissued

    Quality management system EU MDR

    Certifier
    DEKRA Certification GmbH 0124
    Issued
    1 Sep 2026
    Expires
    28 Sep 2031
    Valid from
    29 Sep 2026

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Dental Treatment Units
Model / Reference
1.010.7050
Primary DI / UDI-DI
EKAV101070500
Basic UDI-DI
++EKAVG001YA
EMDN Code
Z12110101 Dental treatment units
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006471

Other devices from KaVo Dental GmbH

See all devices from KaVo Dental GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: 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