Skip to content

Dornier UIMS

by Dornier MedTech GmbH 14 variants

Ref K1049991

Dornier UIMS (K1049991) is a Class IIb device made by Dornier Medtech GmbH, registered in EUDAMED on 18 Nov 2022 (Basic UDI-DI 4049957DornierUIMSAN), 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 Number4049957DornierUIMSAN Basic UDI-DI 04049957006679UDI-DIDate18 Nov 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
K1049991
Primary DI / UDI-DI
04049957006679
Basic UDI-DI
4049957DornierUIMSAN
Direct marketing DI
04049957006679
EMDN code
Z12030201 Central information computing systems
Device class
Class IIb
Special device type
Software
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009774

Similar devices in this category

Other devices filed under CENTRAL INFORMATION COMPUTING SYSTEMS.

Other devices from Dornier Medtech GmbH

See all devices from Dornier Medtech GmbH →

Properties

Other properties (14, all answered No)