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Depth Gauge

by Proi̇mtech Sağlik Ürünleri̇ Anoni̇m Şi̇rketi̇

Ref DGModel Depth Gauge

Active European Union

CE MDR

Valid until

21 May 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2614202 Date22 May 2026IssuedStatusActive expires 21 May 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2614202 Active

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    22 May 2026
    Expires
    21 May 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Dental Hand Tools
Model / Reference
Depth Gauge, DG
Primary DI / UDI-DI
08681489710073
Basic UDI-DI
86814897prohndtoolsImZH
Direct Marketing DI
08681489710073
EMDN Code
Z12119099 Various dental stomatology instruments - other
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020130

Other devices from Proi̇mtech Sağlik Ürünleri̇ Anoni̇m Şi̇rketi̇

See all devices from Proi̇mtech Sağlik Ürünleri̇ Anoni̇m Şi̇rketi̇ →

Properties

  • Reusable
  • Measuring Function

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No