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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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Probenahme- und Einsende-Kit Atemgas — 4 UDI-DI variants, IVDR

MD Atlas
Cerascreen GmbH

Data from EUDAMED, last updated May 23, 2026

Probenahme- und Einsende-Kit Atemgas

42516207007K3

4 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Cerascreen GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 42516207007K3
Device name: Probenahme- und Einsende-Kit Atemgas
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Cerascreen GmbH
SRN: DE-MF-000017602
Country: Germany
Email: fragen@cerascreen.de
Phone: +49 385 3936322 2

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HF77H9A320YQ1222SDHNYAXA

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

cerascreen® Fructose Intolerance Test04251620707237
9901014804251620708623
9901003404251620708616
9901003304251620700306