Skip to content

Kürette

by Geister Medizintechnik GmbH 875 variants

Part of a family of 886 devices: see the family page

Ref UT2300-15

Kürette (UT2300-15) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 40570340000000522MW), 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 Number40570340000000522MW Basic UDI-DI 04057034269329UDI-DIDate8 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Kürette
Model / reference
UT2300-15
Primary DI / UDI-DI
04057034269329
Basic UDI-DI
40570340000000522MW
Direct marketing DI
04057034269329
EMDN code
L0315 General surgery dissectors, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005461

Similar devices in this category

Other devices filed under GENERAL SURGERY DISSECTORS, REUSABLE.

Other devices from Geister Medizintechnik GmbH

See all devices from Geister Medizintechnik GmbH →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)