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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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Eurotube EVA parenteral bags — 3 UDI-DI variants, MDR (Eurozyto GmbH)

MD Atlas
Eurozyto GmbH

Data from EUDAMED, last updated May 23, 2026

Eurotube EVA parenteral bags

42607383314001LS

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Eurozyto GmbH

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 42607383314001LS
Device name: Eurotube EVA parenteral bags
Device model: TPN EVA UV Bags, multichambers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eurozyto GmbH
SRN: DE-MF-000008373
Country: Germany
Email: b.hau@eurozyto.de
Phone: +49 1705867353

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KGPTWX1ARQK1Q8ETE62YY3V7

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

TPN EVA UV bag Heptatube04260738330015
TPN EVA UV bag Nonatube04260738330022
TPN EVA UV bag Oktatube04260738330039