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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 Delta III — 6 UDI-DI variants, MDR (Dornier MedTech GmbH)

MD Atlas
Dornier MedTech GmbH

Data from EUDAMED, last updated May 23, 2026

Dornier Delta III

4049957DornierDeltaIIIF5

6 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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UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01G10V0QYJ0FG1K0T6KGX13G9N

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

K104393604049957006167
K104393504049957006150
K104593604049957006457
K104593904049957006488
K104593504049957006440
K104594004049957006495

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4049957DornierDeltaIIIF5
Device name: Dornier Delta III
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 7, 2022

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