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ME Diamant

by Edenta Etablissement 14 variants

Ref 889ME.314.007Model 16670

ME Diamant (889ME.314.007) is a Class IIa device made by Edenta Etablissement, registered in EUDAMED on 2 Feb 2022 (Basic UDI-DI ++E31216670EL) with CE/MDR certificate 1000183128 valid until 26 Mar 2030, active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

26 Mar 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000183128 Date27 Mar 2025IssuedStatusActive expires 26 Mar 2030

Official records

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

Timeline

3 dated events

  1. Registered EUDAMED ++E31216670EL
  2. Certificate issued EUDAMED 1000183128
  3. Certificate expires EUDAMED 1000183128

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Diamant Instrumente
Model / reference
16670, 889ME.314.007
Primary DI / UDI-DI
E312889ME3140071
Basic UDI-DI
++E31216670EL
Unit of use DI
E312889ME314007101
EMDN code
Z12110102 Dental drills
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Liechtenstein

Manufacturer details

EUDAMED SRN
LI-MF-000011937

Similar devices in this category

Other devices filed under INSTRUMENTS FOR DENTAL TREATMENT UNITS.

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Properties

  • Sterilise before use
Other properties (13, all answered No)