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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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RUDADERM® — 6 UDI-DI variants, MDR (NOBAMED Paul Danz AG)

MD Atlas
NOBAMED Paul Danz AG

Data from EUDAMED, last updated May 23, 2026

RUDADERM®

4031815081303W

6 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: NOBAMED Paul Danz AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4031815081303W
Device name: RUDADERM®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: NOBAMED Paul Danz AG
SRN: DE-MF-000000023
Country: Germany
Email: info@nobamed-ag.com
Phone: +49 0 2335 7609 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KH8X41B85MTZ9C9FACDF5PW6

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

09009404031815081324
09010504031815081522
09020604031815081720
09030704031815083724
09110504031815091521
09120604031815091729