Skip to content

Sonde

by Geister Medizintechnik GmbH 90 variants

Part of a family of 91 devices: see the family page

Ref 41-1015.DF

Sonde (41-1015.DF) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 405703400000011ZS), 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 Number405703400000011ZS Basic UDI-DI 04057034503416UDI-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  • Withdrawn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
Sonde
Model / reference
41-1015.DF
Primary DI / UDI-DI
04057034503416
Basic UDI-DI
405703400000011ZS
Direct marketing DI
04057034503416
EMDN code
L031102 Exploration probes, 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 EXPLORATION PROBES, 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)