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Dilatator

by Geister Medizintechnik GmbH 37 variants

Part of a family of 156 devices: see the family page

Ref 21-0235

Dilatator (21-0235) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 405703400000002ZR), 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 Number405703400000002ZR Basic UDI-DI 04057034048399UDI-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  • Withdrawn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
Dilatator
Model / reference
21-0235
Primary DI / UDI-DI
04057034048399
Basic UDI-DI
405703400000002ZR
Direct marketing DI
04057034048399
EMDN code
L070802 Vascular dilators, 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 CARDIOVASCULAR SURGERY INSTRUMENTS, 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)