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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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Infusionsleitungen — 1 UDI-DI variant, MDR (CARDEA GmbH & Co. KG)

MD Atlas
CARDEA GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Infusionsleitungen

426059063000010A9

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: CARDEA GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426059063000010A9
Device name: Infusionsleitungen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: CARDEA GmbH & Co. KG
SRN: DE-MF-000006460
Country: Germany
Email: info@cardea-med.de
Phone: 0049 39424 940090

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01GSD44NZ63KY8B8WM8P5SHYFZ

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

2580280T04260590631572