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MEDENTiKA

by Medentika GmbH 322 variants

Part of a family of 82 devices: see the family page

Ref 4-13-11Model Placement instrument

MEDENTiKA (4-13-11) is a Class IIa device made by MEDENTiKA GmbH, registered in EUDAMED on 29 Jul 2026 (Basic UDI-DI 42515748PLA002D2), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42515748PLA002D2 Basic UDI-DI 04251574847492UDI-DIDate29 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Placement instrument, 4-13-11
Primary DI / UDI-DI
04251574847492
Basic UDI-DI
42515748PLA002D2
EMDN code
L159099 Odontostomatology instruments, reusable - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009117

Similar devices in this category

Other devices filed under ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER.

Other devices from MEDENTiKA GmbH

See all devices from MEDENTiKA GmbH →

Properties

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