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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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Kolibri comtrain PREMIUM — 11 UDI-DI variants, MDR

MD Atlas
Igefa Handelsgesellschaft mbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Kolibri comtrain PREMIUM

4024009216595169YL

11 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Igefa Handelsgesellschaft mbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4024009216595169YL
Device name: Kolibri comtrain PREMIUM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Igefa Handelsgesellschaft mbH & Co. KG
SRN: DE-MF-000029971
Country: Germany
Email: info@igefa.de
Phone: +49 (0) 33394 51-0

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KDNAJMFCP8B3YGW5CCQFGQGJ

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

216595504024009029899
216595304024009029875
216595104024009029851
216595704024009029912
216596904024009013614
216596704024009013591
216596304024009029974
216596104024009029950
216595904024009029936
216596504024009029998
218281304024009174100