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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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Schläuche — 5 UDI-DI variants, MDR (ASSKEA GmbH)

MD Atlas
ASSKEA GmbH

Data from EUDAMED, last updated May 23, 2026

Schläuche

426058604Tubing8H

5 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: ASSKEA GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426058604Tubing8H
Device name: Schläuche
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: ASSKEA GmbH
SRN: DE-MF-000005146
Country: Germany
Email: mps@asskea.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KQS4S8BCYJDG7D4CWV5V6MZW

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

Connecting tube disposable secretion canister system04260586040401
Connecting tube for "OneWay" secretion container system04260586041835
connection tube reusable secretion canister04260586041590
Connection tube reusable secretion canister04260586040371
45879404260586041620