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Stanze

by Geister Medizintechnik GmbH 869 variants

Ref 40-1420A4

Stanze (40-1420A4) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 405703400000013ZW), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number405703400000013ZW Basic UDI-DI 04057034142271UDI-DIDate9 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Stanze
Model / reference
40-1420A4
Primary DI / UDI-DI
04057034142271
Basic UDI-DI
405703400000013ZW
Direct marketing DI
04057034142271
EMDN code
L091302 Bone rongeurs, 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

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Properties

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