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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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Cardiohelp II Venous Probe — 2 UDI-DI variants, MDR

MD Atlas
Maquet Cardiopulmonary GmbH

Data from EUDAMED, last updated May 23, 2026

Cardiohelp II Venous Probe

405886332915DP

2 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: Maquet Cardiopulmonary GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 405886332915DP
Device name: Cardiohelp II Venous Probe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Maquet Cardiopulmonary GmbH
SRN: DE-MF-000020091
Country: Germany
Email: raop.cp@getinge.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K8805ZG4EJT711CPJMMZK7TK

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

Cardiohelp II Venous Probe04058863329154
Cardiohelp II Venous Probe04058863329154