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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 comfort PREMIUM — 4 UDI-DI variants, MDR

MD Atlas
Igefa Handelsgesellschaft mbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Kolibri comfort PREMIUM

4024009216503137UN

4 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: 4024009216503137UN
Device name: Kolibri comfort PREMIUM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 23, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KD570WMBN4E47W1EFXDJ6XG8

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

216503704024009013249
216503104024009013034
216503504024009013225
216503304024009013188