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

MD Atlas
RoweMed AG - Medical 4 Life

Data from EUDAMED, last updated May 23, 2026

RowePaed

42503476PAEDJL

4 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: 42503476PAEDJL
Device name: RowePaed
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZWBBTCARG7EKFWMF1FPA42F

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

A-660004250347605154
A-660604250347604904
A-660204250347604898
A-660104250347604881