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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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SCHUTZAUFLAGE/ -UNTERLAGE — 13 UDI-DI variants, MDR

MD Atlas
NOBAMED Paul Danz AG

Data from EUDAMED, last updated May 23, 2026

SCHUTZAUFLAGE/ -UNTERLAGE

4031815683005Z

13 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: 4031815683005Z
Device name: SCHUTZAUFLAGE/ -UNTERLAGE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJYRFHVTXTBM2R4RA98KDNBD

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

66917504031815682729
66921004031815683122
66814004031815681425
66614004031815683429
66914004031815682422
66817504031815681722
66617504031815683726
66717504031815684723
66721004031815685126
66821004031815682125
66621004031815684129
66921104031815683221
67007904031815680824