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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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Holder — 6 UDI-DI variants, MDR (Maquet Cardiopulmonary GmbH)

MD Atlas
Maquet Cardiopulmonary GmbH

Data from EUDAMED, last updated May 23, 2026

Holder

405886357664FE

6 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: Maquet Cardiopulmonary GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 405886357664FE
Device name: Holder
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 20, 2026

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KHXNQ4CXDF6X59H20XHYGJ13

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

016061 Holder arm04037691576640
016062 Holder for Oxygenator04037691009025
HKH 7900 Holder for PLS-i oxygenator04037691108841
HKH 8870 Holder for priming bag04037691588285
HKHZ 19 Single holder oxygenat. neo/ped04037691533339
HKHZ 27 Adapter for oxygenator neo/ped04037691753430