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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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Kolibri2 — 42 UDI-DI variants, MDR (Greggersen Gasetechnik GmbH)

MD Atlas
Greggersen Gasetechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Kolibri2

4031196KOLIBRIR7

42 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Greggersen Gasetechnik GmbH

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 4031196KOLIBRIR7
Device name: Kolibri2
Device model: Flowmeter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Greggersen Gasetechnik GmbH
SRN: DE-MF-000006442
Country: Germany
Email: ra@greggersen.de

Variants by status

UDI-DI variants

42 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KE9DRHFFVBS4Z1GPZXGMVD3N

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

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90640404031196009689
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90645404031196010425
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90640304031196009672
90642204031196009818
90641004031196009733
90643504031196010326
90645604031196010449
90645004031196010395
90640204031196009665

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