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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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Entnahmehalm — 3 UDI-DI variants, MDR (RoweMed AG - Medical 4 Life)

MD Atlas
RoweMed AG - Medical 4 Life

Data from EUDAMED, last updated May 23, 2026

Entnahmehalm

42503476ENTNAHMEHALMM2

3 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: RoweMed AG - Medical 4 Life

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503476ENTNAHMEHALMM2
Device name: Entnahmehalm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01FYXFTQ1Q2ZG2C96BTDCT9X08

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

RowePhil 3/5.0 - Filterstraw 100 mm04250347603068
RowePhil 3/5.0 - Filterstraw 100 mm, 5,0 µm PET mesh, PUR Ø 1,5x2,7 mm14250347605700
RoweWithdrawalStraw04250347602597