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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Dornier UIMS — 14 UDI-DI variants, MDR (Dornier MedTech GmbH)

MD Atlas
Dornier MedTech GmbH

Data from EUDAMED, last updated May 23, 2026

Dornier UIMS

4049957DornierUIMSAN

14 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Dornier MedTech GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4049957DornierUIMSAN
Device name: Dornier UIMS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: Dornier MedTech GmbH
SRN: DE-MF-000009774
Country: Germany
Email: eudamed@dornier.com
Phone: +49 8153 888 0

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJ50H5P92BMPBY7JYM3C3GYB

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

K104822104049957006556
K104746804049957006532
K104748504049957006525
K104683704049957006334
K104700504049957006358
K104570304049957006198
Dornier UIMS04049957006679
K105135704049957006907
K105029504049957006693
K1049044 04049957006624
K105089904049957006884
K104623804049957006228
K104935004049957006655
K104744304049957006433