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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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disposable secretion canister system — 7 UDI-DI variants, MDR

MD Atlas
ASSKEA GmbH

Data from EUDAMED, last updated May 23, 2026

disposable secretion canister system

426058604Bag-OneWayYH

7 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: 426058604Bag-OneWayYH
Device name: disposable secretion canister system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 20, 2022

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01G8DD7R0ZV9G4CH8Z1D0SNEFK

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

"Bag" external container (1000 ml)04260586041705
disposable liner "OneWay" (1 l)04260586040197
Disposable liner "OneWay" (1 l)04260586041712
external canister "Bag"04260586040289
external canister "Bag" (1 l)04260586041606
external canister "Bag" (1 l)04260586041637
external container 1000 ml04260586041514