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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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Transfusionssysteme — 7 UDI-DI variants, MDR

MD Atlas
RoweMed AG - Medical 4 Life

Data from EUDAMED, last updated May 23, 2026

Transfusionssysteme

42503476TRANSFUSIONCE

7 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: RoweMed AG - Medical 4 Life

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503476TRANSFUSIONCE
Device name: Transfusionssysteme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: RoweMed AG - Medical 4 Life
SRN: DE-MF-000005350
Country: Germany
Email: info@rowemed.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01FZW5FP9BKQYEZ4FH4CAVYZYW

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

600104250347605574
600304250347605567
A-3104/1504250347605727
05600304250347604201
A-310004250347603266
RoweTrans ExtensionLine04250347603235
RoweTransfusionLine04250347603327