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Exa Special RA - gelb

by Edenta Etablissement 3 variants

Ref 0735RA-25Model 16412

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte 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 Number1000183128 Date27 Mar 2025IssuedStatusWithdrawn No longer placed on the EU market expires 26 Mar 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000183128 Active

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    27 Mar 2025
    Expires
    26 Mar 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Polierer / Arkansas
Model / Reference
16412, 0735RA-25
Primary DI / UDI-DI
E3120735RA251
Basic UDI-DI
++E31216412DU
Unit of Use DI
E3120735RA25101
EMDN Code
Q01010403 Dental abrasive and polishing materials
Device Class
Class IIa
EU market of registration
Liechtenstein

Manufacturer details

EUDAMED SRN
LI-MF-000011937

Other devices from Edenta Etablissement

See all devices from Edenta Etablissement →

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