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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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X-RAY-RINGTUPFER — 6 UDI-DI variants, MDR (NOBAMED Paul Danz AG)

MD Atlas
NOBAMED Paul Danz AG

Data from EUDAMED, last updated May 23, 2026

X-RAY-RINGTUPFER

40318158710066

6 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: NOBAMED Paul Danz AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40318158710066
Device name: X-RAY-RINGTUPFER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 15, 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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Export results

Applied filters

basicUdiUlid01KF0PWPFEJ7XJCK0KZRVDGWNT

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

87141204031815871123
87142004031815871222
87142504031815871321
87143304031815871420
87144004031815871529
87145004031815871628